Crosstalk between ESKAPE bacteria and NK cells: mutual regulation and role in developing reproductive tract pathologies
- Authors: Grebenkina P.V.1,2, Selkov S.A.1, Kraeva L.А.2,3, Sokolov D.I.1,2
-
Affiliations:
- The Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott
- Saint Petersburg Pasteur Institute
- Military Medical Academy named after S.M. Kirov
- Issue: Vol 13, No 4 (2023)
- Pages: 609-626
- Section: REVIEWS
- URL: https://journals.rcsi.science/2220-7619/article/view/158868
- DOI: https://doi.org/10.15789/2220-7619-CBE-15452
- ID: 158868
Cite item
Full Text
Abstract
Natural killer (NK) cells represent one of the innate lymphoid cell subsets, which are often studied in the context of antitumor and antiviral immunity, as well as due to their localization in the zone of the mother-fetus contact (in the uterus), therefore underlying their extensive investigation in developing pregnancy. At the same time, their role in antibacterial immune response has been poorly examined. Because NK cells can produce cytokines, one of putative options for their participation in eliminating prokaryotic pathogens may be coupled to regulation of immune system cells such as dendritic cells, macrophages, etc. However, there have been also described variants of contact cytolysis of cells infected with intracellular bacteria enabled due to cytotoxic proteins — perforin, granzymes, granulisin found in NK cells. In recent years, it has become known that NK cells take part in development of immune response against extracellular bacteria including the ESKAPE group bacteria, which includes opportunistic prokaryotes that most actively develop antibiotic resistance and cause nosocomial infections. Here, we attempted to review the data on the role NK cells play in antibacterial immunity. Assessing a crosstalk between ESKAPE group bacteria and NK cells also attracts researchers due to the ability of prokaryotes to alter functions of immune cells, but very little is known about the effects they exert on NK cells. At the same time, such data could be applied to seek out for new ways to treat oncological diseases as well as pave the basis for new approaches to regulating NK cell characteristics in reproductive pathologies. As mentioned earlier, the latter occur in the decidual membrane, where they can interact with fetal cells including trophoblast cells. It is believed that cells can mutually regulate each other’s properties necessary for the course of physiological pregnancy. Probably, imbalance in this system can lead to development of reproductive pathologies. The review summarizes the currently available data on the effects of ESKAPE group bacteria on NK cells, and also considers putative mechanisms for emergence of impaired interaction between NK cells and trophoblasts exposed to ESKAPE group bacteria. Owing to few publications available on this phenomenon, the experimental study assessing an impact of ESKAPE group bacteria on NK cell properties is envisioned as a necessary stage in development of contemporary biology.
Full Text
##article.viewOnOriginalSite##About the authors
Polina V. Grebenkina
The Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott; Saint Petersburg Pasteur Institute
Author for correspondence.
Email: grebenkinap@gmail.com
ORCID iD: 0000-0002-5229-9732
Junior Researcher, PhD Student
Russian Federation, 199034, Saint Petersburg, Mendeleyevskaya line, 3; 197101, Saint Petersburg, st. Mira, 14Sergey A. Selkov
The Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott
Email: selkovsa@mail.ru
ORCID iD: 0000-0003-1560-7529
DSc (Medicine), Professor, Head of the Department of Immunology and Intercellular Interactions
Russian Federation, 199034, Saint Petersburg, Mendeleyevskaya line, 3Lyudmila А. Kraeva
Saint Petersburg Pasteur Institute; Military Medical Academy named after S.M. Kirov
Email: lykraeva@yandex.ru
ORCID iD: 0000-0002-9115-3250
DSc (Medicine), Head of the Laboratory of Medical Bacteriology, Professor of the Department of Microbiology
Russian Federation, 197101, Saint Petersburg, st. Mira, 14; Saint PetersburgDmitriy I. Sokolov
The Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott; Saint Petersburg Pasteur Institute
Email: falcojugger@yandex.ru
ORCID iD: 0000-0002-5749-2531
DSc (Biology), Associate Professor, Head of Laboratory of Intercellular Interactions, Researcher, Laboratory of Molecular Immunology
Russian Federation, 199034, Saint Petersburg, Mendeleyevskaya line, 3; 197101, Saint Petersburg, st. Mira, 14References
- Малышкина Д.А., Анциферова Ю.С., Долгушина Н.В. Особенности экспрессии рецепторов семейства NCR в популяции эндометриальных естественных киллеров у пациенток с лейомиомой матки // Российский иммунологический журнал. 2019. Т. 22, № 2-1. C. 391–393. [Malyshkina D.A., Antsiferova Yu.S., Dolgushina N.V. The expresiion of NCR receptors by endometrial natural killers in women with uterine leiomyoma. Rossiiskii immunologicheskii zhurnal = Russian Journal of Immunology, 2019, vol. 22, no. 2-1, pp. 391–393. (In Russ.)] doi: 10.31857/S102872210006907-2
- Мерфи К., Уивер К. Иммунобиология по Джанвэю. М.: Логосфера, 2020. 1184 с. [Murphy K., Weaver K. Immunobiology by Janway. Moscow: Logosphere, 2020. 1184 p. (In Russ.)]
- Abbas Y., Oefner C.M., Polacheck W.J., Gardner L., Farrell L., Sharkey A., Kamm R., Moffett A., Oyen M.L. A microfluidics assay to study invasion of human placental trophoblast cells. J. R. Soc. Interface, 2017, vol. 14, no. 130: 20170131. doi: 10.1098/rsif.2017.0131
- Ahmadi M., Ghaebi M., Abdolmohammadi-Vahid S., Abbaspour-Aghdam S., Hamdi K., Abdollahi-Fard S., Danaii S., Mosapour P., Koushaeian L., Dolati S., Rikhtegar R., Oskouei F.D., Aghebati-Maleki L., Nouri M., Yousefi M. NK cell frequency and cytotoxicity in correlation to pregnancy outcome and response to IVIG therapy among women with recurrent pregnancy loss. J. Cell. Physiol., 2018, vol. 234, no. 6, pp. 9428–9437. doi: 10.1002/jcp.27627
- Andersson M., Gunne H., Agerberth B., Boman A., Bergman T., Sillard R., Jörnvall H., Mutt V., Olsson B., Wigzell H. NK-lysin, a novel effector peptide of cytotoxic T and NK cells. Structure and cDNA cloning of the porcine form, induction by interleukin 2, antibacterial and antitumour activity. EMBO J., 1995, vol. 14, no. 8, pp. 1615–1625. doi: 10.1002/j.1460-2075.1995.tb07150.x
- Ao X., Gan Q., Huang X., Bao D., Wu X., Lin Q., Lin A., Ding Y., Wang L., Chen Y., Huang Z. TLR8 agonist partially improves IFNγ deficiency of NK cells in chronic hepatitis B through the synergy of monocytes. Aliment. Pharmacol. Ther., 2022, vol. 57, no. 4, pp. 387–398. doi: 10.1111/apt.17382
- Augusto L.A., Bourgeois-Nicolaos N., Breton A., Barreault S., Alonso E.H., Gera S., Faraut-Derouin V., Semaan N., De Luca D., Chaby R., Doucet-Populaire F., Tissières P. Presence of 2-hydroxymyristate on endotoxins is associated with death in neonates with Enterobacter cloacae complex septic shock. iScience, 2021, vol. 24, no. 8: 102916. doi: 10.1016/j.isci.2021.102916
- Avendaño-Ortiz J., Llanos-González E., Toledano V., del Campo R., Cubillos-Zapata C., Lozano-Rodríguez R., Ismail A., Prados C., Gómez-Campelo P., Aguirre L.A., García-Río F., López-Collazo E. Pseudomonas aeruginosa colonization causes PD-L1 overexpression on monocytes, impairing the adaptive immune response in patients with cystic fibrosis. J. Cyst. Fibros., 2019, vol. 18, no. 5, pp. 630–635. doi: 10.1016/j.jcf.2018.11.002
- Ayobami O., Willrich N., Reuss A., Eckmanns T., Markwart R. The ongoing challenge of vancomycin-resistant Enterococcus faecium and Enterococcus faecalis in Europe: an epidemiological analysis of bloodstream infections. Emerg. Microbes Infect., 2020, vol. 9, no. 1, pp. 1180–1193. doi: 10.1080/22221751.2020.1769500
- Bae J.S., Da F., Liu R., He L., Lv H., Fisher E.L., Rajagopalan G., Li M., Cheung G.Y.C., Otto M. Contribution of Staphylococcal enterotoxin B to Staphylococcus aureus systemic infection. J. Infect. Dis., 2021, vol. 223, no. 10, pp. 1766–1775. doi: 10.1093/infdis/jiaa584
- Balle C., Esra R., Havyarimana E., Jaumdally S.Z., Lennard K., Konstantinus I.N., Barnabas S.L., Happel A.U., Gill K., Pidwell T., Lingappa J.R., Gamieldien H., Bekker L.G., Passmore J.S., Jaspan H.B. Relationship between the oral and vaginal microbiota of South African adolescents with high prevalence of bacterial vaginosis. Microorganisms, 2020, vol. 8, no. 7: 1004. doi: 10.3390/microorganisms8071004
- Bengoechea J.A., Sa Pessoa J. Klebsiella pneumoniae infection biology: living to counteract host defences. FEMS Microbiol. Rev., 2019, vol. 43, no. 2, pp. 123–144. doi: 10.1093/femsre/fuy043
- Bernardy E.E., Petit R.A., Raghuram V., Alexander A.M., Read T.D., Goldberg J.B., Harwood C.S. Genotypic and phenotypic diversity of Staphylococcus aureus isolates from cystic fibrosis patient lung infections and their interactions with Pseudomonas aeruginosa. mBio, 2020, vol. 11, no. 3: e00735-20. doi: 10.1128/mBio.00735-20
- Boucher H.W., Talbot G.H., Bradley J.S., Edwards J.E., Gilbert D., Rice L.B., Scheld M., Spellberg B., Bartlett J. Bad bugs, no drugs: no ESKAPE! An update from the Infectious Diseases Society of America. Clin. Infect. Dis., 2009, vol. 48, no. 1, pp. 1–12. doi: 10.1086/595011
- Brennan T.V., Lin L., Brandstadter J.D., Rendell V.R., Dredge K., Huang X., Yang Y. Heparan sulfate mimetic PG545-mediated antilymphoma effects require TLR9-dependent NK cell activation. J. Clin. Invest., 2016, vol. 126, no. 1, pp. 207–219. doi: 10.1172/JCI76566
- Cai G., Kastelein R.A., Hunter C.A. IL-10 enhances NK cell proliferation, cytotoxicity and production of IFN-gamma when combined with IL-18. Eur. J. Immunol., 1999, vol. 29, no. 9, pp. 2658–2665. doi: 10.1002/(SICI)1521-4141(199909)29:09<2658::AID-IMMU2658>3.0.CO;2-G
- Cai S., Wang J., Wang K., Chen D., Dong X., Liu T., Zeng Y., Wang X., Wu D. Expression, purification and antibacterial activity of NK-lysin mature peptides from the channel catfish (Ictalurus punctatus). Appl. Sci., 2016, vol. 6, no. 9: 240. doi: 10.3390/app6090240
- Caneiras C., Lito L., Melo-Cristino J., Duarte A. Community- and hospital-acquired Klebsiella pneumoniae urinary tract infections in portugal: virulence and antibiotic resistance. Microorganisms, 2019, vol. 7, no. 5: 138. doi: 10.3390/microorganisms7050138
- Cavalcanti Y.V.N., Brelaz M.C.A., Lemoine Neves J.K.d.A., Ferraz J.C., Pereira V.R.A. Role of TNF-alpha, IFN-gamma, and IL-10 in the development of pulmonary tuberculosis. Pulm. Med., 2012, vol. 2012: 745483. doi: 10.1155/2012/745483
- Chalifour A., Jeannin P., Gauchat J.F., Blaecke A., Malissard M., N’Guyen T., Thieblemont N., Delneste Y. Direct bacterial protein PAMP recognition by human NK cells involves TLRs and triggers alpha-defensin production. Blood, 2004, vol. 104, no. 6, pp. 1778–1783. doi: 10.1182/blood-2003-08-2820
- Chambers H.F. The changing epidemiology of Staphylococcus aureus? Emerg. Infect. Dis., 2001, vol. 7, no. 2, pp. 178–182. doi: 10.3201/eid0702.010204
- Chen L., Yi L., Ren Y., Zhang J., Kinghorn A.D., Caligiuri M.A., Yu J. Enhancement of natural killer cell interferon-gamma production by the derivatives of the natural product phyllanthusmins via TLR-mediated NF-kb and STAT3 signaling pathways. Blood, 2015, vol. 126, no. 23, pp. 1031–1031. doi: 10.1182/blood.V126.23.1031.1031
- Chung J.W., Piao Z.H., Yoon S.R., Kim M.S., Jeong M., Lee S.H., Min J.K., Kim J.W., Cho Y.H., Kim J.C., Ahn J.K., Kim K.E., Choi I. Pseudomonas aeruginosa eliminates natural killer cells via phagocytosis-induced apoptosis. PLoS Pathog., 2009, vol. 5, no. 8: e1000561. doi: 10.1371/journal.ppat.1000561
- Cimpean M., Cooper M.A. Metabolic regulation of NK cell antiviral functions during cytomegalovirus infection. J. Leuk. Biol., 2023, vol. 113, no. 5, pp. 525–534. doi: 10.1093/jleuko/qiad018
- Comin F., Speziali E., Martins-Filho O.A., Caldas I.R., Moura V., Gazzinelli A., Correa-Oliveira R., Faria A.M.C. Ageing and Toll-like receptor expression by innate immune cells in chronic human schistosomiasis. Clin. Exp. Immunol., 2007, vol. 149, no. 2, pp. 274–284. doi: 10.1111/j.1365-2249.2007.03403.x
- Cong Y., Yang S., Rao X. Vancomycin resistant Staphylococcus aureus infections: a review of case updating and clinical features. J. Adv. Res., 2020, vol. 21, pp. 169–176. doi: 10.1016/j.jare.2019.10.005
- Coombs G.W., Daley D.A., Thin Lee Y., Pang S., Pearson J.C., Robinson J.O., Johnson P.D., Kotsanas D., Bell J.M., Turnidge J.D., Australian Group on Antimicrobial R. Australian Group on Antimicrobial Resistance Australian Enterococcal Sepsis Outcome Programme annual report, 2014. Commun. Dis. Intell. Q Rep., 2016, vol. 40, no. 2, pp. E236–E243.
- Cortez V.S., Fuchs A., Cella M., Gilfillan S., Colonna M. Cutting edge: salivary gland NK cells develop independently of Nfil3 in steady-state. J. Immunol., 2014, vol. 192, no. 10, pp. 4487–4491. doi: 10.4049/jimmunol.1303469
- Dadashi M., Hajikhani B., Darban-Sarokhalil D., van Belkum A., Goudarzi M. Mupirocin resistance in Staphylococcus aureus: a systematic review and meta-analysis. J. Glob. Antimicrob. Resist., 2020, vol. 20, pp. 238–247. doi: 10.1016/j.jgar.2019.07.032
- Davin-Regli A., Lavigne J.P., Pages J.M. Enterobacter spp.: update on taxonomy, clinical aspects, and emerging antimicrobial resistance. Clin. Microbiol. Rev., 2019, vol. 32, no. 4: e00002-19. doi: 10.1128/CMR.00002-19
- De Oliveira D.M.P., Forde B.M., Phan M.-D., Steiner B., Zhang B., Zuegg J., El-deeb I.M., Li G., Keller N., Brouwer S., Harbison-Price N., Cork A.J., Bauer M.J., Alquethamy S.F., Beatson S.A., Roberts J.A., Paterson D.L., McEwan A.G., Blaskovich M.A.T., Schembri M.A., McDevitt C.A., von Itzstein M., Walker M.J., Ballard J.D. Rescuing tetracycline class antibiotics for the treatment of multidrug-resistant Acinetobacter baumannii pulmonary infection. mBio, 2022, vol. 13, no. 1: e0351721. doi: 10.1128/mbio.03517-21
- Devi C.A., Ranjani A., Dhanasekaran D., Thajuddin N., Ramanidevi T. Surveillance of multidrug resistant bacteria pathogens from female infertility cases. Afr. J. Biotechnol., 2013, vol. 12, no. 26, pp. 4129–4134. doi: 10.5897/AJB2013.12507
- Dons’koi B.V., Chernyshov V.P., Sirenko V.Y., Strelko G.V., Osypchuk D.V. Peripheral blood natural killer cells activation status determined by CD69 upregulation predicts implantation outcome in IVF. Immunobiology, 2014, vol. 219, no. 3, pp. 167–171. doi: 10.1016/j.imbio.2013.09.002
- Ebbo M., Gérard L., Carpentier S., Vély F., Cypowyj S., Farnarier C., Vince N., Malphettes M., Fieschi C., Oksenhendler E., Schleinitz N., Vivier E. Low circulating natural killer cell counts are associated with severe disease in patients with common variable immunodeficiency. EBioMedicine, 2016, vol. 6, pp. 222–230. doi: 10.1016/j.ebiom.2016.02.025
- Eckert L.O., Moore D.E., Patton D.L., Agnew K.J., Eschenbach D.A. Relationship of vaginal bacteria and inflammation with conception and early pregnancy loss following in-vitro fertilization. Infect. Dis. Obstet. Gynecol., 2003, vol. 11, no. 1, pp. 11–17. doi: 10.1155/S1064744903000024
- El Zowalaty M.E., Al Thani A.A., Webster T.J., El Zowalaty A.E., Schweizer H.P., Nasrallah G.K., Marei H.E., Ashour H.M. Pseudomonas aeruginosa: arsenal of resistance mechanisms, decades of changing resistance profiles, and future antimicrobial therapies. Future Microbiol., 2015, vol. 10, no. 10, pp. 1683–706. doi: 10.2217/fmb.15.48
- Enright M.C., Robinson D.A., Randle G., Feil E.J., Grundmann H., Spratt B.G. The evolutionary history of methicillin-resistant Staphylococcus aureus (MRSA). Proc. Natl Acad. Sci. USA, 2002, vol. 99, no. 11, pp. 7687–7692. doi: 10.1073/pnas.122108599
- Eriksson M., Meadows S.K., Basu S., Mselle T.F., Wira C.R., Sentman C.L. TLRs mediate IFN-gamma production by human uterine NK cells in endometrium. J. Immunol., 2006, vol. 176, no. 10, pp. 6219–6224. doi: 10.4049/jimmunol.176.10.6219
- Feasey N.A., Garner P., Hamer D.H., Dramowski A., van Ginneken N., Musicha P., Lester R. Prevalence and outcome of bloodstream infections due to third-generation cephalosporin-resistant Enterobacteriaceae in sub-Saharan Africa: a systematic review. J. Antimicrob. Chemother., 2020, vol. 75, no. 3, pp. 492–507. doi: 10.1093/jac/dkz464
- Fu Q., Maniar A., Quevedo Diaz M., Chapoval A.I., Medvedev A.E. Activation of cytokine-producing and antitumor activities of natural killer cells and macrophages by engagement of Toll-like and NOD-like receptors. Innate Immunity, 2010, vol. 17, no. 4, pp. 375–387. doi: 10.1177/1753425910372000
- Fukui A., Funamizu A., Fukuhara R., Shibahara H. Expression of natural cytotoxicity receptors and cytokine production on endometrial natural killer cells in women with recurrent pregnancy loss or implantation failure, and the expression of natural cytotoxicity receptors on peripheral blood natural killer cells in pregnant women with a history of recurrent pregnancy loss. J. Obstet. Gynaecol. Res., 2017, vol. 43, no. 11, pp. 1678–1686. doi: 10.1111/jog.13448
- Gan L., Yan C., Cui J., Xue G., Fu H., Du B., Zhao H., Feng J., Feng Y., Fan Z., Mao P., Fu T., Xu Z., Du S., Liu S., Zhang R., Zhang Q., Li N., Cui X., Li X., Zhou Y., Huang L., Yuan J., Teo J.W.P. Genetic diversity and pathogenic features in Klebsiella pneumoniae isolates from patients with pyogenic liver abscess and pneumonia. Microbiol. Spectr., 2022, vol. 10, no. 2: e0264621. doi: 10.1128/spectrum.02646-21
- Gao W., Howden B.P., Stinear T.P. Evolution of virulence in Enterococcus faecium, a hospital-adapted opportunistic pathogen. Curr. Opin. Microbiol., 2018, vol. 41, pp. 76–82. doi: 10.1016/j.mib.2017.11.030
- García-Laorden M.I., Stroo I., Blok D.C., Florquin S., Medema J.P., de Vos A.F., van der Poll T. Granzymes A and B regulate the local inflammatory response during Klebsiella pneumoniae pneumonia. J. Innate Immun., 2016, vol. 8, no. 3, pp. 258–268. doi: 10.1159/000443401
- Girardin S.E., Tournebize R., Mavris M., Page A.L., Li X., Stark G.R., Bertin J., DiStefano P.S., Yaniv M., Sansonetti P.J., Philpott D.J. CARD4/Nod1 mediates NF-κB and JNK activation by invasive Shigella flexneri. EMBO Rep., 2001, vol. 2, no. 8, pp. 736–742. doi: 10.1093/embo-reports/kve155
- Giuliani E., Parkin K.L., Lessey B.A., Young S.L., Fazleabas A.T. Characterization of uterine NK cells in women with infertility or recurrent pregnancy loss and associated endometriosis. Am. J. Reprod. Immunol., 2014, vol. 72, no. 3, pp. 262–269. doi: 10.1111/aji.12259
- Goldenson B.H., Zhu H., Wang Y.M., Heragu N., Bernareggi D., Ruiz-Cisneros A., Bahena A., Ask E.H., Hoel H.J., Malmberg K.-J., Kaufman D.S. Umbilical cord blood and iPSC-derived natural killer cells demonstrate key differences in cytotoxic activity and KIR profiles. Front. Immunol., 2020, vol. 11, no. doi: 10.3389/fimmu.2020.561553
- Gorrie C., Higgs C., Carter G., Stinear T.P., Howden B. Genomics of vancomycin-resistant Enterococcus faecium. Microb. Genom., 2019, vol. 5, no. 7: e000283. doi: 10.1099/mgen.0.000283
- Graham C.H., Lysiak J.J., McCrae K.R., Lala P.K. Localization of transforming growth factor-beta at the human fetal-maternal interface: role in trophoblast growth and differentiation. Biol. Reprod., 1992, vol. 46, no. 4, pp. 561–572. doi: 10.1095/biolreprod46.4.561
- Grebenkina P.V., Mikhailova V.A., Oshkolova A.A., Vershinina S.O., Dukhinova M.S., Bazhenov D.O., Selkov S.A., Sokolov D.I. Decidual natural killer cells and trophoblast cells: cellular, humoral and molecular mechanisms of interaction. Medical Immunology (Russia), 2022, vol. 24, no. 6, pp. 1085–1108. doi: 10.15789/1563-0625-dnk-2540
- Groslambert M., Py B. Spotlight on the NLRP3 inflammasome pathway. J. Inflam. Res., 2018, vol. 11, pp. 359–374. doi: 10.2147/jir.S141220
- Guan Z., Liu Y., Liu C., Wang H., Feng J., Yang G. Staphylococcus aureus β-hemolysin up-regulates the expression of IFN-γ by human CD56bright NK сells. Front. Cell. Infect. Microbiol., 2021, vol. 11 : 658141. doi: 10.3389/fcimb.2021.658141
- Halabian R., Jahangiri A., Sedighian H., Behzadi E., Fooladi A.A.I. Staphylococcal enterotoxin B as DNA vaccine against breast cancer in a murine model. Int. Microbiol., 2023: pp. 1–11. doi: 10.1007/s10123-023-00348-y
- Haller D., Clements J.D., Blum S., Bode C., Hammes W.P., Schiffrin E.J. Activation of human peripheral blood mononuclear cells by nonpathogenic bacteria in vitro: evidence of NK cells as primary targets. Infect. Immun., 2000, vol. 68, no. 2, pp. 752–759. doi: 10.1128/iai.68.2.752-759.2000
- Han C., Li H., Han L., Wang C., Yan Y., Qi W., Fan A., Wang Y., Xue F. Aerobic vaginitis in late pregnancy and outcomes of pregnancy. Eur. J. Clin. Microbiol. Infect. Dis., 2019, vol. 38, no. 2, pp. 233–239. doi: 10.1007/s10096-018-3416-2
- Hart O.M., Athie-Morales V., O’Connor G.M., Gardiner C.M. TLR7/8-mediated activation of human NK cells results in accessory cell-dependent IFN-γ production. J. Immunol., 2005, vol. 175, no. 3, pp. 1636–1642. doi: 10.4049/jimmunol.175.3.1636
- Hayakawa Y., Screpanti V., Yagita H., Grandien A., Ljunggren H.-G., Smyth M.J., Chambers B.J. NK cell TRAIL eliminates immature dendritic cells in vivo and limits dendritic cell vaccination efficacy. J. Immunol., 2004, vol. 172, no. 1, pp. 123–129. doi: 10.4049/jimmunol.172.1.123
- He S., Chu J., Wu L.-C., Mao H., Peng Y., Alvarez-Breckenridge C.A., Hughes T., Wei M., Zhang J., Yuan S., Sandhu S., Vasu S., Benson D.M., C. Hofmeister C., He X., Ghoshal K., Devine S.M., Caligiuri M.A., Yu J. MicroRNAs activate natural killer cells through Toll-like receptor signaling. Blood, 2013, vol. 121, no. 23, pp. 4663–4671. doi: 10.1182/blood-2012-07-441360
- He T., Tang C., Xu S., Moyana T., Xiang J. Interferon gamma stimulates cellular maturation of dendritic cell line DC2.4 leading to induction of efficient cytotoxic T cell responses and antitumor immunity. Cell. Mol. Immunol., 2007, vol. 4, no. 2, pp. 105–111.
- Hoffmann S.C., Cohnen A., Ludwig T., Watzl C. 2B4 engagement mediates rapid LFA-1 and actin-dependent NK cell adhesion to tumor cells as measured by single cell force spectroscopy. J. Immunol., 2011, vol. 186, no. 5, pp. 2757–2764. doi: 10.4049/jimmunol.1002867
- Hou F., Peng L., Jiang J., Chen T., Xu D., Huang Q., Ye C., Peng Y., Hu D.-L., Fang R. ATP facilitates ыtaphylococcal enterotoxin O шnduced neutrophil IL-1β secretion via NLRP3 inflammasome dependent pathways. Front. Immunol., 2021, vol. 12: 649235. doi: 10.3389/fimmu.2021.649235
- Huang Y., Rana A.P., Wenzler E., Ozer E.A., Krapp F., Bulitta J.B., Hauser A.R., Bulman Z.P. Aminoglycoside-resistance gene signatures are predictive of aminoglycoside MICs for carbapenem-resistant Klebsiella pneumoniae. J. Antimicrob. Chemother., 2022, vol. 77, no. 2, pp. 356–363. doi: 10.1093/jac/dkab381
- Huebner J., Fischetti V.A., Wang Y., Krueger W.A., Madoff L.C., Martirosian G., Boisot S., Goldmann D.A., Kasper D.L., Tzianabos A.O., Pier G.B. isolation and chemical characterization of a capsular polysaccharide antigen shared by clinical isolates of Enterococcus faecalis and vancomycin-resistant Enterococcus faecium. Infect. Immun., 1999, vol. 67, no. 3, pp. 1213–1219. doi: 10.1128/iai.67.3.1213-1219.1999
- Ivin M., Dumigan A., de Vasconcelos F.N., Ebner F., Borroni M., Kavirayani A., Przybyszewska K.N., Ingram R.J., Lienenklaus S., Kalinke U., Stoiber D., Bengoechea J.A., Kovarik P. Natural killer cell-intrinsic type I IFN signaling controls Klebsiella pneumoniae growth during lung infection. PLoS Pathog., 2017, vol. 13, no. 11: e1006696. doi: 10.1371/journal.ppat.1006696
- Jabbari Shiadeh S.M., Pormohammad A., Hashemi A., Lak P. Global prevalence of antibiotic resistance in blood-isolated Enterococcus faecalis and Enterococcus faecium: a systematic review and meta-analysis. Infect. Drug. Resist., 2019, vol. 12, pp. 2713–2725. doi: 10.2147/IDR.S206084
- Jiang W., Li X., Wen M., Liu X., Wang K., Wang Q., Li Y., Zhou M., Liu M., Hu B., Zeng H. Increased percentage of PD-L1+ natural killer cells predicts poor prognosis in sepsis patients: a prospective observational cohort study. Crit. Care, 2020, vol. 24, no. 1: 617. doi: 10.1186/s13054-020-03329-z
- Jiao L., Gao X., Joyee A.G., Zhao L., Qiu H., Yang M., Fan Y., Wang S., Yang X. NK cells promote type 1 T cell immunity through modulating the function of dendritic cells during intracellular bacterial infection. J. Immunol., 2011, vol. 187, no. 1, pp. 401–411. doi: 10.4049/jimmunol.1002519
- Joji R., Al Rashed N., Saeed N., Bindayna K. Detection of overexpression of efflux pump expression in fluoroquinolone-resistant Pseudomonas aeruginosa isolates. Int. J. Appl. Basic. Med. Res., 2020, vol. 10, no. 1, pp. 37-42. doi: 10.4103/ijabmr.IJABMR_90_19
- Kamoshida G., Akaji T., Takemoto N., Suzuki Y., Sato Y., Kai D., Hibino T., Yamaguchi D., Kikuchi-Ueda T., Nishida S., Unno Y., Tansho-Nagakawa S., Ubagai T., Miyoshi-Akiyama T., Oda M., Ono Y. Lipopolysaccharide-deficient Acinetobacter baumannii due to colistin resistance is killed by neutrophil-produced lysozyme. Front. Microbiol., 2020, vol. 11, no. doi: 10.3389/fmicb.2020.00573
- Kanter J., Gordon S.M., Mani S., Sokalska A., Park J.Y., Senapati S., Huh D.D., Mainigi M. Hormonal stimulation reduces numbers and impairs function of human uterine natural killer cells during implantation. Hum Reprod., 2023, vol. 38, no. 6, pp. 1047–1059. doi: 10.1093/humrep/dead069
- Khalifa S.M., Abd El-Aziz A.M., Hassan R., Abdelmegeed E.S. β-lactam resistance associated with β-lactamase production and porin alteration in clinical isolates of E. coli and K. pneumoniae. PLoS One, 2021, vol. 16, no.5: e0251594. doi: 10.1371/journal.pone.0251594
- Kathirvel S., Mani M., Gopala Krishnan G.K., Sethumadhavan A., Vijayalakshmi T., Ponnan S.M., Hanna L.E., Mathaiyan M. Molecular characterization of Enterococcus faecalis isolates from urinary tract infection and interaction between Enterococcus faecalis encountered Dendritic and Natural Killer cells. Microb. Pathog., 2020, vol. 140: 103944. doi: 10.1016/j.micpath.2019.103944
- Kaya E., Grassi L., Benedetti A., Maisetta G., Pileggi C., Di Luca M., Batoni G., Esin S. In vitro interaction of Pseudomonas aeruginosa biofilms with human peripheral blood mononuclear cells. Front. Cell. Infect. Microbiol., 2020, vol. 10: 187. doi: 10.3389/fcimb.2020.00187
- Khalili Y., Yekani M., Goli H.R., Memar M.Y. Characterization of carbapenem-resistant but cephalosporin-susceptible Pseudomonas aeruginosa. Acta Microbiol Immunol Hung., 2019, vol. 66, no. 4, pp. 529–540. doi: 10.1556/030.66.2019.036
- Khanmohammadi S., Rezaei N. CAR-NK cells: a promising cellular immunotherapy in lymphoma. Expert Opin. Biol. Ther., 2022, vol. 23, no. 1, pp. 37–47. doi: 10.1080/14712598.2022.2154601
- Kim B., Wang Y.-C., Hespen C.W., Espinosa J., Salje J., Rangan K.J., Oren D.A., Kang J.Y., Pedicord V.A., Hang H.C. Enterococcus faecium secreted antigen A generates muropeptides to enhance host immunity and limit bacterial pathogenesis. eLife, 2019, vol. 8: e45343. doi: 10.7554/eLife.45343
- Klimpel G.R., Niesel D.W., Klimpel K.D. Natural cytotoxic effector cell activity against Shigella flexneri-infected HeLa cells. J. Immunol., 1986, vol. 136, no. 3, pp. 1081–1086.
- Kopcow H.D., Allan D.S., Chen X., Rybalov B., Andzelm M.M., Ge B., Strominger J.L. Human decidual NK cells form immature activating synapses and are not cytotoxic. Proc. Natl Acad. Sci. USA, 2005, vol. 102, no. 43, pp. 15563–15568.
- Korenevsky A.V., Shcherbitskaia A.D., Berezkina M.E., Markova K.L., Alexandrova E.P., Balabas O.A., Selkov S.A., Sokolov D.I. MALDI-TOF mass spectrometric protein profiling of microvesicles produced by the NK-92 natural killer cell line. Medical Immunology (Russia), 2020, vol. 22, no. 4, pp. 633–646. doi: 10.15789/1563-0625-MMS-1976
- Kuon R.J., Togawa R., Vomstein K., Weber M., Goeggl T., Strowitzki T., Markert U.R., Zimmermann S., Daniel V., Dalpke A.H., Toth B. Higher prevalence of colonization with Gardnerella vaginalis and gram-negative anaerobes in patients with recurrent miscarriage and elevated peripheral natural killer cells. J. Reproduct. Immunol., 2017, vol. 120, pp. 15–19. doi: 10.1016/j.jri.2017.03.001
- Kussmann M., Karer M., Obermueller M., Schmidt K., Barousch W., Moser D., Nehr M., Ramharter M., Poeppl W., Makristathis A., Winkler S., Thalhammer F., Burgmann H., Lagler H. Emergence of a dalbavancin induced glycopeptide/lipoglycopeptide non-susceptible Staphylococcus aureus during treatment of a cardiac device-related endocarditis. Emerg. Microbes. Infect., 2018, vol. 7, no. 1: 202. doi: 10.1038/s41426-018-0205-z
- Lash G.E., Otun H.A., Innes B.A., Kirkley M., De Oliveira L., Searle R.F., Robson S.C., Bulmer J.N. Interferon-gamma inhibits extravillous trophoblast cell invasion by a mechanism that involves both changes in apoptosis and protease levels. FASEB J., 2006, vol. 20, no. 14, pp. 2512–2518. doi: 10.1096/fj.06-6616com
- Leavis H.L., Bonten M.J., Willems R.J. Identification of high-risk enterococcal clonal complexes: global dispersion and antibiotic resistance. Curr. Opin. Microbiol., 2006, vol. 9, no. 5, pp. 454–460. doi: 10.1016/j.mib.2006.07.001
- Lee B.C., Kim M.S., Pae M., Yamamoto Y., Eberlé D., Shimada T., Kamei N., Park H.S., Sasorith S., Woo J.R., You J., Mosher W., Brady H.J., Shoelson S.E., Lee J. Adipose natural killer cells regulate adipose tissue macrophages to promote insulin resistance in obesity. Cell Metabolism, 2016, vol. 23, no. 4, pp. 685–698. doi: 10.1016/j.cmet.2016.03.002
- Lee V.T., Feehan D.D., Jamil K., Polyak M.J., Ogbomo H., Hasell M., Li S.S., Xiang R.F., Parkins M., Trapani J.A., Harrison J.J., Mody C.H. Natural killer cells kill extracellular Pseudomonas aeruginosa using contact-dependent release of granzymes B and H. PLoS Pathog., 2022, vol. 18, no. 2: e1010325. doi: 10.1371/journal.ppat.1010325
- Li P., Sheng Q., Huang L.C., Turner J.H. Epithelial innate immune response to Pseudomonas aeruginosa-derived flagellin in chronic rhinosinusitis. Int Forum Allergy Rhinol., 2023. doi: 10.1002/alr.23164
- Librach C.L., Feigenbaum S.L., Bass K.E., Cui T.Y., Verastas N., Sadovsky Y., Quigley J.P., French D.L., Fisher S.J. Interleukin-1 beta regulates human cytotrophoblast metalloproteinase activity and invasion in vitro. J. Biol. Chem., 1994, vol. 269, no. 25, pp. 17125–17131.
- Liesenborghs L., Meyers S., Lox M., Criel M., Claes J., Peetermans M., Trenson S., Vande Velde G., Vanden Berghe P., Baatsen P., Missiakas D., Schneewind O., Peetermans W.E., Hoylaerts M.F., Vanassche T., Verhamme P. Staphylococcus aureus endocarditis: distinct mechanisms of bacterial adhesion to damaged and inflamed heart valves. Eur. Heart J., 2019, vol. 40, no. 39, pp. 3248–3259. doi: 10.1093/eurheartj/ehz175
- Liu F.-T., Yang S., Yang Z., Zhou P., Peng T., Yin J., Ye Z., Shan H., Yu Y., Li R., Auchtung J.M. An altered microbiota in the lower and upper female reproductive tract of women with recurrent spontaneous abortion. Microbiol. Spectr., 2022, vol. 10, no. 3: e0046222 10.1128/spectrum.00462-22
- Liu Z.-Y., Yang H.-L., Wei C.-Y., Cai G.-H., Ye J.-D., Zhang C.-X., Sun Y.-Z. Commensal Bacillus siamensis LF4 induces antimicrobial peptides expression via TLRs and NLRs signaling pathways in intestinal epithelial cells of Lateolabrax maculatus. Fish Shellfish Immunol., 2023, vol. 134: 108634. doi: 10.1016/j.fsi.2023.108634
- Lotzová E., Herberman R. Immunobiology of natural killer cells. Boca Raton, 2019. doi: 10.1201/9780429288364
- Louis E., Galloway-Peña J., Roh J.H., Latorre M., Qin X., Murray B.E. Genomic and SNP analyses demonstrate a distant separation of the hospital and community-associated clades of Enterococcus faecium. PLoS One, 2012, vol. 7, no. 1: e30187. doi: 10.1371/journal.pone.0030187
- Lowy F.D. Antimicrobial resistance: the example of Staphylococcus aureus. J. Clin. Invest., 2003, vol. 111, no. 9, pp. 1265–1273. doi: 10.1172/JCI18535
- Luger T.A., Krutmann J., Kirnbauer R., Urbanski A., Schwarz T., Klappacher G., Kock A., Micksche M., Malejczyk J., Schauer E., et al. IFN-beta 2/IL-6 augments the activity of human natural killer cells. J. Immunol., 1989, vol. 143, no. 4, pp. 1206–1209.
- Mace E.M., Dongre P., Hsu H.T., Sinha P., James A.M., Mann S.S., Forbes L.R., Watkin L.B., Orange J.S. Cell biological steps and checkpoints in accessing NK cell cytotoxicity. Immunol. Cell. Biol., 2014, vol. 92, no. 3, pp. 245–255. doi: 10.1038/icb.2013.96
- Mammina C., Bonura C., di Carlo P., Calà C., Aleo A., Monastero R., Palma D.M. Daptomycin non-susceptible, vancomycin intermediate methicillin-resistant Staphylococcus aureus ST398 from a chronic leg ulcer, Italy. Scand. J. Infect. Dis., 2010, vol. 42, no. 11–12, pp. 955–957. doi: 10.3109/00365548.2010.524662
- Manaster I., Mizrahi S., Goldman-Wohl D., Sela H.Y., Stern-Ginossar N., Lankry D., Gruda R., Hurwitz A., Bdolah Y., Haimov-Kochman R., Yagel S., Mandelboim O. Endometrial NK cells are special immature cells that await pregnancy. J. Immunol., 2008, vol. 181, no. 3, pp. 1869–1876. doi: 10.4049/jimmunol.181.3.1869
- Markovska R., Stoeva T., Dimitrova D., Boyanova L., Stankova P., Mihova K., Mitov I. Quinolone resistance mechanisms among third-generation cephalosporin resistant isolates of Enterobacter spp. in a Bulgarian university hospital. Infect. Drug Resist., 2019, vol. 12, pp. 1445–1455. doi: 10.2147/idr.S204199
- Mateos M., Hernández-García M., del Campo R., Martínez-García L., Gijón D., Morosini M.I., Ruiz-Garbajosa P., Cantón R. Emergence and persistence over time of carbapenemase-producing Enterobacter isolates in a Spanish University Hospital in Madrid, Spain (2005–2018). Microb. Drug Resist., 2021, vol. 27, no. 7, pp. 895–903. doi: 10.1089/mdr.2020.0265
- Matheeussen V., Xavier B.B., Mermans I., De Weerdt A., Lammens C., Goossens H., Jansens H., Malhotra-Kumar S. Emergence of colistin resistance during treatment of recurrent pneumonia caused by carbapenemase producing Klebsiella pneumoniae. Diagn. Microbiol. Infect. Dis., 2019, vol. 94, no. 4, pp. 407–409. doi: 10.1016/j.diagmicrobio.2019.02.014
- McConnell M.J., Actis L., Pachon J. Acinetobacter baumannii: human infections, factors contributing to pathogenesis and animal models. FEMS Microbiol. Rev., 2013, vol. 37, no. 2, pp. 130–155. doi: 10.1111/j.1574-6976.2012.00344.x
- Meunier E., Broz P. Evolutionary convergence and divergence in NLR function and structure. Trends Immunol., 2017, vol. 38, no. 10, pp. 744–757. doi: 10.1016/j.it.2017.04.005
- Michałkiewicz J., Stachowski J., Barth C., Patzer J., Dzierżanowska D., Madaliński K. Effect of Pseudomonas aeruginosa exotoxin A on IFN-γ synthesis: expression of costimulatory molecules on monocytes and activity of NK cells. Immunol. Lett., 1999, vol. 69, no. 3, pp. 359–366. doi: 10.1016/s0165-2478(99)00121-2
- Mikhailova V., Grebenkina P., Khokhlova E., Davydova A., Salloum Z., Tyshchuk E., Zagainova V., Markova K., Kogan I., Selkov S., Sokolov D. Pro- and anti-inflammatory cytokines in the context of NK cell-trophoblast interactions. Int. J. Mol. Sci., 2022, vol. 23, no. 4: 2387. doi: 10.3390/ijms23042387
- Mikhailova V., Khokhlova E., Grebenkina P., Salloum Z., Nikolaenkov I., Markova K., Davidova A., Selkov S., Sokolov D. NK-92 cells change their phenotype and function when cocultured with IL-15, IL-18 and trophoblast cells. Immunobiology, 2021, vol. 226, no. 5: 152125. doi: 10.1016/j.imbio.2021.152125
- Mirandola P., Ponti C., Gobbi G., Sponzilli I., Vaccarezza M., Cocco L., Zauli G., Secchiero P., Manzoli F.A., Vitale M. Activated human NK and CD8+ T cells express both TNF-related apoptosis-inducing ligand (TRAIL) and TRAIL receptors but are resistant to TRAIL-mediated cytotoxicity. Blood, 2004, vol. 104, no. 8, pp. 2418–2424. doi: 10.1182/blood-2004-04-1294
- Mohd Sazlly Lim S., Zainal Abidin A., Liew S.M., Roberts J.A., Sime F.B. The global prevalence of multidrug-resistance among Acinetobacter baumannii causing hospital-acquired and ventilator-associated pneumonia and its associated mortality: a systematic review and meta-analysis. J. Infect., 2019, vol. 79, no. 6, pp. 593–600. doi: 10.1016/j.jinf.2019.09.012
- Molgora M., Cortez V.S., Colonna M. Killing the invaders: NK cell impact in tumors and anti-tumor therapy. Cancers (Basel), 2021, vol. 13, no. 4. doi: 10.3390/cancers13040595
- Montaldo E., Del Zotto G., Della Chiesa M., Mingari M.C., Moretta A., De Maria A., Moretta L. Human NK cell receptors/markers: a tool to analyze NK cell development, subsets and function. Cytometry A, 2013, vol. 83, no. 8, pp. 702–713. doi: 10.1002/cyto.a.22302
- Mourenza Á., Gil J.A., Mateos L.M., Letek M. Novel treatments and preventative strategies against food-poisoning caused by Staphylococcal species. Pathogens, 2021, vol. 10, no. 2: 91. doi: 10.3390/pathogens10020091
- Mulani M.S., Kamble E.E., Kumkar S.N., Tawre M.S., Pardesi K.R. Emerging strategies to combat ESKAPE pathogens in the era of antimicrobial resistance: a review. Front. Microbiol., 2019, vol. 10: 539. doi: 10.3389/fmicb.2019.00539
- Naveed M., Jabeen K., Naz R., Mughal M.S., Rabaan A.A., Bakhrebah M.A., Alhoshani F.M., Aljeldah M., Shammari B.R.A., Alissa M., Sabour A.A., Alaeq R.A., Alshiekheid M.A., Garout M., Almogbel M.S., Halwani M.A., Turkistani S.A., Ahmed N. Regulation of host immune response against Enterobacter cloacae proteins via computational mRNA vaccine design through transcriptional modification. Microorganisms, 2022, vol. 10, no. 8: 1621. doi: 10.3390/microorganisms10081621
- Nelson D.B., Hanlon A.L., Wu G., Liu C., Fredricks D.N. First trimester levels of BV-associated bacteria and risk of miscarriage among women early in pregnancy. Matern. Child Health J., 2015, vol. 19, no. 12, pp. 2682–2687. doi: 10.1007/s10995-015-1790-2
- Opoku-Temeng C., Kobayashi S.D., DeLeo F.R. Klebsiella pneumoniae capsule polysaccharide as a target for therapeutics and vaccines. Comput. Struct. Biotechnol. J., 2019, vol. 17, pp. 1360–1366. doi: 10.1016/j.csbj.2019.09.011
- Orfali R.L., Yoshikawa F.S.Y., Oliveira L.M.D.S., Pereira N.Z., de Lima J.F., Ramos Y.Á.L., Duarte A.J.D.S., Sato M.N., Aoki V. Staphylococcal enterotoxins modulate the effector CD4+ T cell response by reshaping the gene expression profile in adults with atopic dermatitis. Sci. Rep., 2019, vol. 9, no. 1: 13082. doi: 10.1038/s41598-019-49421-5
- Otun H.A., Lash G.E., Innes B.A., Bulmer J.N., Naruse K., Hannon T., Searle R.F., Robson S.C. Effect of tumour necrosis factor-α in combination with interferon-γ on first trimester extravillous trophoblast invasion. J. Reproduct. Immunol., 2011, vol. 88, no. 1, pp. 1–11. doi: 10.1016/j.jri.2010.10.003
- Parodi M., Favoreel H., Candiano G., Gaggero S., Sivori S., Mingari M.C., Moretta L., Vitale M., Cantoni C. NKp44-NKp44 ligand interactions in the regulation of natural killer cells and other innate lymphoid cells in humans. Front. Immunol., 2019, vol. 10: 719. doi: 10.3389/fimmu.2019.00719
- Paul S., Lal G. the molecular mechanism of natural killer cells function and its importance in cancer immunotherapy. Front. Immunol., 2017, vol. 8: 1124. doi: 10.3389/fimmu.2017.01124
- Pechere J.C., Kohler T. Patterns and modes of beta-lactam resistance in Pseudomonas aeruginosa. Clin. Microbiol. Infect., 1999, vol. 5, suppl. 1, pp. S15–S18. doi: 10.1111/j.1469-0691.1999.tb00719.x
- Pedersen B.K., Kharazmi A. Inhibition of human natural killer cell activity by Pseudomonas aeruginosa alkaline protease and elastase. Infect. Immun., 1987, vol. 55, no. 4, pp. 986–989. doi: 10.1128/iai.55.4.986-989.1987
- Peng H., Wisse E., Tian Z. Liver natural killer cells: subsets and roles in liver immunity. Cell. Mol. Immunol., 2015, vol. 13, no. 3, pp. 328–336. doi: 10.1038/cmi.2015.96
- Peri F., Piazza M., Calabrese V., Damore G., Cighetti R. Exploring the LPS/TLR4 signal pathway with small molecules. Biochem. Soc. Trans., 2010, vol. 38, no. 5, pp. 1390–1395. doi: 10.1042/bst0381390
- Pfaller M.A., Cormican M., Flamm R.K., Mendes R.E., Jones R.N. Temporal and geographic variation in antimicrobial susceptibility and resistance patterns of Enterococci: results from the SENTRY antimicrobial surveillance program, 1997–2016. Open Forum Infect. Dis., 2019, vol. 6, suppl. 1, pp. S54–S62. doi: 10.1093/ofid/ofy344
- Prince A., Lacey K.A., Mulcahy M.E., Towell A.M., Geoghegan J.A., McLoughlin R.M. Clumping factor B is an important virulence factor during Staphylococcus aureus skin infection and a promising vaccine target. PLoS Pathog., 2019, vol. 15, no. 4: e1007713. doi: 10.1371/journal.ppat.1007713
- Prutsch N., Fock V., Haslinger P., Haider S., Fiala C., Pollheimer J., Knofler M. The role of interleukin-1beta in human trophoblast motility. Placenta, 2012, vol. 33, no. 9, pp. 696–703. doi: 10.1016/j.placenta.2012.05.008
- Quatrini L., Della Chiesa M., Sivori S., Mingari M.C., Pende D., Moretta L. Human NK cells, their receptors and function. Eur. J. Immunol., 2021, vol. 51, no. 7, pp. 1566–1579. doi: 10.1002/eji.202049028
- Rice L.B. Federal funding for the study of antimicrobial resistance in nosocomial pathogens: no ESKAPE. J. Infect. Dis., 2008, vol. 197, no. 8, pp. 1079–1081. doi: 10.1086/533452
- Roussev R.G., Dons’koi B.V., Stamatkin C., Ramu S., Chernyshov V.P., Coulam C.B., Barnea E.R. Preimplantation factor inhibits circulating natural killer cell cytotoxicity and reduces CD69 expression: implications for recurrent pregnancy loss therapy. Reprod. Biomed. Online, 2013, vol. 26, no. 1, pp. 79–87. doi: 10.1016/j.rbmo.2012.09.017
- Salim F., Gunawan H., Suwarsa O., Sutedja E. Increased expression of Toll-Like Receptor (TLR) 2 and TLR6 on peripheral blood monocytes by induction of Staphylococcal enterotoxin B during exacerbation of atopic dermatitis patients. Clin. Cosmet. Investig. Dermatol., 2023, vol. 16, pp. 301–307. doi: 10.2147/ccid.S401815
- Salmanov A.G., Ishchak O.M., Shostak Y.M., Kozachenko V.V., Rud V.O., Golyanovskiy O.V., Shkorbotun V.O. Bacterial infection causes of pregnancy loss and premature birth in the women in Ukraine. Wiadomości Lekarskie, 2021, vol. 74, no. 6, pp. 1355–1359. doi: 10.36740/WLek202106113
- Schlievert P.M., Davis C.C. Device-associated menstrual toxic shock syndrome. Clin. Microbiol. Rev., 2020, vol. 33, no. 3: e00032-19. doi: 10.1128/cmr.00032-19
- Schönian G., Fernández-Figueroa E.A., Imaz-Rosshandler I., Castillo-Fernández J.E., Miranda-Ortíz H., Fernández-López J.C., Becker I., Rangel-Escareño C. Down-regulation of TLR and JAK/STAT pathway genes is associated with diffuse cutaneous leishmaniasis: a gene expression analysis in NK cells from patients infected with Leishmania mexicana. PLoS Negl. Trop. Dis., 2016, vol. 10, no. 3: e0004570. doi: 10.1371/journal.pntd.0004570
- Screpanti V., Wallin R.P.A., Grandien A., Ljunggren H.-G. Impact of FASL-induced apoptosis in the elimination of tumor cells by NK cells. Mol. Immunol., 2005, vol. 42, no. 4, pp. 495–499. doi: 10.1016/j.molimm.2004.07.033
- Shekhar S., Peng Y., Gao X., Joyee A.G., Wang S., Bai H., Zhao L., Yang J., Yang X. NK cells modulate the lung dendritic cell-mediated Th1/Th17 immunity during intracellular bacterial infection. Eur. J. Immunol., 2015, vol. 45, no. 10, pp. 2810–2820. doi: 10.1002/eji.201445390
- Singh S., Almuhanna Y., Alshahrani M.Y., Lowman D.W., Rice P.J., Gell C., Ma Z., Graves B., Jackson D., Lee K., Juarez R., Koranteng J., Muntaka S., Daniel A.M., da Silva A.C., Hussain F., Yilmaz G., Mastrotto F., Irie Y., Williams P., Williams D.L., Cámara M., Martinez-Pomares L. Carbohydrates from Pseudomonas aeruginosa biofilms interact with immune C-type lectins and interfere with their receptor function. NPJ Biofilms Microbiomes, 2021, vol. 7, no. 1: 87. doi: 10.1038/s41522-021-00257-w
- Sivori S., Vacca P., Del Zotto G., Munari E., Mingari M.C., Moretta L. Human NK cells: surface receptors, inhibitory checkpoints, and translational applications. Cell. Mol. Immunol., 2019, vol. 16, no. 5, pp. 430–441. doi: 10.1038/s41423-019-0206-4
- Slater C.L., Winogrodzki J., Fraile-Ribot P.A., Oliver A., Khajehpour M., Mark B.L. Adding insult to injury: mechanistic basis for how AmpC mutations allow Pseudomonas aeruginosa to accelerate cephalosporin hydrolysis and evade avibactam. Antimicrob. Agents. Chemother., 2020, vol. 64, no. 9: e00894-20. doi: 10.1128/aac.00894-20
- Small C.L., McCormick S., Gill N., Kugathasan K., Santosuosso M., Donaldson N., Heinrichs D.E., Ashkar A., Xing Z. NK cells play a critical protective role in host defense against acute extracellular Staphylococcus aureus bacterial infection in the lung. J. Immunol., 2008, vol. 180, no. 8, pp. 5558–5568. doi: 10.4049/jimmunol.180.8.5558
- Smoke S.M., Brophy A., Reveron S., Iovleva A., Kline E.G., Marano M., Miller L.P., Shields R.K. Evolution and transmission of Cefiderocol-resistant Acinetobacter baumannii during an outbreak in the burn intensive care unit. Clin. Infect. Dis., 2023, vol. 76, no. 3, pp. e1261–e1265. doi: 10.1093/cid/ciac647
- Sparo M., Delpech G., Batisttelli S., Basualdo J.Á. Immunomodulatory properties of cell wall extract from Enterococcus faecalis CECT7121. Braz. J. Infect. Dis., 2014, vol. 18, no. 5, pp. 551–555. doi: 10.1016/j.bjid.2014.05.005
- Stewart A.G., Paterson D.L., Young B., Lye D.C., Davis J.S., Schneider K., Yilmaz M., Dinleyici R., Runnegar N., Henderson A., Archuleta S., Kalimuddin S., Forde B.M., Chatfield M.D., Bauer M.J., Lipman J., Harris-Brown T., Harris P.N.A., Chia P.Y., Cross G., Somani J., Yan G. Meropenem versus piperacillin-tazobactam for definitive treatment of bloodstream infections caused by AmpC β-lactamase-producing Enterobacter spp., Citrobacter freundii, Morganella morganii, Providencia spp., or Serratia marcescens: a pilot multicenter randomized controlled trial (MERINO-2). Open Forum Infect. Dis., 2021, vol. 8, no. 8: ofab387. doi: 10.1093/ofid/ofab387
- Strateva T., Yordanov D. Pseudomonas aeruginosa — a phenomenon of bacterial resistance. J. Med. Microbiol., 2009, vol. 58, pt 9, pp. 1133–1148. doi: 10.1099/jmm.0.009142-0
- Sun J., Yang M., Ban Y., Gao W., Song B., Wang Y., Zhang Y., Shao Q., Kong B., Qu X. Tim-3 Is Upregulated in NK cells during early pregnancy and Inhibits NK cytotoxicity toward trophoblast in galectin-9 dependent pathway. PLoS One, 2016, vol. 11, no. 1: e0147186. doi: 10.1371/journal.pone.0147186
- Tacconelli E., Carrara E., Savoldi A., Harbarth S., Mendelson M., Monnet D.L., Pulcini C., Kahlmeter G., Kluytmans J., Carmeli Y., Ouellette M., Outterson K., Patel J., Cavaleri M., Cox E.M., Houchens C.R., Grayson M.L., Hansen P., Singh N., Theuretzbacher U., Magrini N., WHO Pathogens Priority List Working Group. Discovery, research, and development of new antibiotics: the WHO priority list of antibiotic-resistant bacteria and tuberculosis. Lancet. Infect. Dis., 2018, vol. 18, no. 3, pp. 318–327. doi: 10.1016/S1473-3099(17)30753-3
- Tallant T., Deb A., Kar N., Lupica J., de Veer M.J., DiDonato J.A. Flagellin acting via TLR5 is the major activator of key signaling pathways leading to NF-kappa B and proinflammatory gene program activation in intestinal epithelial cells. BMC Microbiol., 2004, vol. 4: 33. doi: 10.1186/1471-2180-4-33
- Tamma P.D., Aitken S.L., Bonomo R.A., Mathers A.J., van Duin D., Clancy C.J. Infectious Diseases Society of America Guidance on the Treatment of AmpC β-lactamase-producing enterobacterales, carbapenem-resistant Acinetobacter baumannii, and Stenotrophomonas maltophilia infections. Clin. Infect. Dis., 2022, vol. 74, no. 12, pp. 2089–2114. doi: 10.1093/cid/ciab1013
- Tan H.X., Yang S.L., Li M.Q., Wang H.Y. Autophagy suppression of trophoblast cells induces pregnancy loss by activating decidual NK cytotoxicity and inhibiting trophoblast invasion. Cell. Commun. Signal., 2020, vol. 18, no. 1: 73. doi: 10.1186/s12964-020-00579-w
- Tarazona R., Lopez-Sejas N., Guerrero B., Hassouneh F., Valhondo I., Pera A., Sanchez-Correa B., Pastor N., Duran E., Alonso C., Solana R. Current progress in NK cell biology and NK cell-based cancer immunotherapy. Cancer. Immunol. Immunother., 2020, vol. 69, no. 5, pp. 879–899. doi: 10.1007/s00262-020-02532-9
- Tsuchiya T., Nakao N., Yamamoto S., Hirai Y., Miyamoto K., Tsujibo H. NK1.1(+) cells regulate neutrophil migration in mice with Acinetobacter baumannii pneumonia. Microbiol. Immunol., 2012, vol. 56, no. 2, pp. 107–116. doi: 10.1111/j.1348-0421.2011.00402.x
- Valore E.V., Park C.H., Quayle A.J., Wiles K.R., McCray P.B. Jr., Ganz T. Human beta-defensin-1: an antimicrobial peptide of urogenital tissues. J. Clin. Invest., 1998, vol. 101, no. 8, pp. 1633–1642. doi: 10.1172/JCI1861
- Van Elssen C.H., Vanderlocht J., Frings P.W., Senden-Gijsbers B.L., Schnijderberg M.C., van Gelder M., Meek B., Libon C., Ferlazzo G., Germeraad W.T., Bos G.M. Klebsiella pneumoniae-triggered DC recruit human NK cells in a CCR5-dependent manner leading to increased CCL19-responsiveness and activation of NK cells. Eur. J. Immunol., 2010, vol. 40, no. 11, pp. 3138–3149. doi: 10.1002/eji.201040496
- Vankayalapati R., Garg A., Porgador A., Griffith D.E., Klucar P., Safi H., Girard W.M., Cosman D., Spies T., Barnes P.F. Role of NK cell-activating receptors and their ligands in the lysis of mononuclear phagocytes infected with an intracellular bacterium. J. Immunol., 2005, vol. 175, no. 7, pp. 4611–4617. doi: 10.4049/jimmunol.175.7.4611
- Vankayalapati R., Wizel B., Weis S.E., Safi H., Lakey D.L., Mandelboim O., Samten B., Porgador A., Barnes P.F. The NKp46 receptor contributes to NK cell lysis of mononuclear phagocytes infected with an intracellular bacterium. J. Immunol., 2002, vol. 168, no. 7, pp. 3451–3457. doi: 10.4049/jimmunol.168.7.3451
- Veneziani I., Alicata C., Pelosi A., Landolina N., Ricci B., D’Oria V., Fagotti A., Scambia G., Moretta L., Maggi E. Toll-like receptor 8 agonists improve NK-cell function primarily targeting CD56(bright)CD16(–) subset. J. Immunother. Cancer, 2022, vol. 10, no. 1: e003385. doi: 10.1136/jitc-2021-003385
- Victor A.R., Weigel C., Scoville S.D., Chan W.K., Chatman K., Nemer M.M., Mao C., Young K.A., Zhang J., Yu J., Freud A.G., Oakes C.C., Caligiuri M.A. Epigenetic and Posttranscriptional Regulation of CD16 Expression during Human NK Cell Development. J. Immunol., 2018, vol. 200, no. 2, pp. 565–572. doi: 10.4049/jimmunol.1701128
- Viel S., Marcais A., Guimaraes F.S., Loftus R., Rabilloud J., Grau M., Degouve S., Djebali S., Sanlaville A., Charrier E., Bienvenu J., Marie J.C., Caux C., Marvel J., Town L., Huntington N.D., Bartholin L., Finlay D., Smyth M.J., Walzer T. TGF-beta inhibits the activation and functions of NK cells by repressing the mTOR pathway. Sci. Signal., 2016, vol. 9, no. 415: 19. doi: 10.1126/scisignal.aad1884
- Wang R., Jaw J.J., Stutzman N.C., Zou Z., Sun P.D. Natural killer cell-produced IFN-gamma and TNF-alpha induce target cell cytolysis through up-regulation of ICAM-1. J. Leukoc. Biol., 2012, vol. 91, no. 2, pp. 299–309. doi: 10.1189/jlb.0611308
- Wesselkamper S.C., Eppert B.L., Motz G.T., Lau G.W., Hassett D.J., Borchers M.T. NKG2D is critical for NK cell activation in host defense against Pseudomonas aeruginosa respiratory infection. J. Immunol., 2008, vol. 181, no. 8, pp. 5481–5489. doi: 10.4049/jimmunol.181.8.5481
- Wolf N.K., Kissiov D.U., Raulet D.H. Roles of natural killer cells in immunity to cancer, and applications to immunotherapy. Nat. Rev. Immunol., 2022, vol. 23, no. 2, pp. 90–105. doi: 10.1038/s41577-022-00732-1
- Wu G., Zhu Q., Zeng J., Gu X., Miao Y., Xu W., Lv T., Song Y. Extracellular mitochondrial DNA promote NLRP3 inflammasome activation and induce acute lung injury through TLR9 and NF-κB. J. Thorac. Dis., 2019, vol. 11, no. 11, pp. 4816–4828. doi: 10.21037/jtd.2019.10.26
- Wu W., Wei L., Feng Y., Xie Y., Zong Z. Precise Species Identification by Whole-Genome Sequencing of Enterobacter Bloodstream Infection, China. Emerg. Infect. Dis., 2021, vol. 27, no. 1, pp. 161–169. doi: 10.3201/eid2701.190154
- Wu X., Jin L.P., Yuan M.M., Zhu Y., Wang M.Y., Li D.J. Human first-trimester trophoblast cells recruit CD56brightCD16– NK cells into decidua by way of expressing and secreting of CXCL12/stromal cell-derived factor 1. J. Immunol., 2005, vol. 175, no. 1, pp. 61–68. doi: 10.4049/jimmunol.175.1.61
- Xie X., Ma L., Zhou Y., Shen W., Xu D., Dou J., Shen B., Zhou C. Polysaccharide enhanced NK cell cytotoxicity against pancreatic cancer via TLR4/MAPKs/NF-κB pathway in vitro/vivo. Carbohydr. Polym., 2019, vol. 225: 115223. doi: 10.1016/j.carbpol.2019.115223
- Xu X., Weiss I.D., Zhang H.H., Singh S.P., Wynn T.A., Wilson M.S., Farber J.M. Conventional NK cells can produce IL-22 and promote host defense in Klebsiella pneumoniae pneumonia. J. Immunol., 2014, vol. 192, no. 4, pp. 1778–1786.
- Yang X., Yang Y., Yuan Y., Liu L., Meng T. The roles of uterine natural killer (NK) cells and KIR/HLA-C combination in the development of preeclampsia: a systematic review. Biomed. Res. Int., 2020, vol. 2020: 4808072. doi: 10.1155/2020/4808072
- Yang Y., Yin C., Pandey A., Abbott D., Sassetti C., Kelliher M.A. NOD2 pathway activation by MDP or Mycobacterium tuberculosis infection involves the stable polyubiquitination of Rip2. J. Biol. Chem., 2007, vol. 282, no. 50, pp. 36223–36229. doi: 10.1074/jbc.M703079200
- Yu J., Caligiuri M.A. Viral- and tumor-reactive natural killer cells. Semin. Immunol., 2023, vol. 67: 101749. doi: 10.1016/ j.smim.2023.101749
- Yu J., Wei M., Becknell B., Trotta R., Liu S., Boyd Z., Jaung M.S., Blaser B.W., Sun J., Benson D.M., Mao H., Yokohama A., Bhatt D., Shen L., Davuluri R., Weinstein M., Marcucci G., Caligiuri M.A. Pro- and antiinflammatory cytokine signaling: reciprocal antagonism regulates interferon-gamma production by human natural killer cells. Immunity, 2006, vol. 24, no. 5, pp. 575–590. doi: 10.1016/j.immuni.2006.03.016
- Zaghi E., Calvi M., Marcenaro E., Mavilio D., Di Vito C. Targeting NKG2A to elucidate natural killer cell ontogenesis and to develop novel immune-therapeutic strategies in cancer therapy. J. Leukoc. Biol., 2019, vol. 105, no. 6, pp. 1243–1251. doi: 10.1002/jlb.Mr0718-300r
- Zhang Y., Huang C., Lian R., Xu J., Fu Y., Zeng Y., Tu W. The low cytotoxic activity of peripheral blood NK cells may relate to unexplained recurrent miscarriage. Am. J. Reprod. Immunol., 2021, vol. 85, no. 6: e13388. doi: 10.1111/aji.13388
- Zheng Y., Valdez P.A., Danilenko D.M., Hu Y., Sa S.M., Gong Q., Abbas A.R., Modrusan Z., Ghilardi N., de Sauvage F.J., Ouyang W. Interleukin-22 mediates early host defense against attaching and effacing bacterial pathogens. Nat. Med., 2008, vol. 14, no. 3, pp. 282–289. doi: 10.1038/nm1720
- Zou M.Z., Liu W.L., Gao F., Bai X.F., Chen H.S., Zeng X., Zhang X.Z. Artificial natural killer cells for specific tumor inhibition and renegade macrophage re-education. Adv. Mater., 2019, vol. 31, no. 43: e1904495. doi: 10.1002/adma.201904495