Порядковый номер ссылки	
Авторы, название публикации и источника, где она опубликована, выходные данные	
ФИО, название публикации и источника на английском	
Полный интернет-адрес (URL) цитируемой статьи или ее doi.	

1	
	
Akinrinmade O.A., Chetty S., Daramola A.K., Islam M.U., Thepen T., Barth S. CD64: An Attractive Immunotherapeutic Target for M1-type Macrophage Mediated Chronic Inflammatory Diseases. Biomedicines, 2017, Vol. 5, no. 3, pii: E56.	
doi: 10.3390/
biomedicines5030056	

2	
	
Bharat A., McQuattie-Pimentel A.C., Budinger G.R.S. Non-classical monocytes in tissue injury and cancer. Oncotarget, 2017, Vol. 8, no. 63, pp. 106171-106172.	
doi: 10.18632/
oncotarget.22584	

3	
	
Biller J.D., Takahashi L.S. Oxidative stress and fish immune system: phagocytosis and leukocyte respiratory burst activity. An. Acad. Bras. Cienc., 2018, Vol. 90, no. 4, pp. 3403-3414.	
doi: 10.1590/0001-3765201820170730	

4	
	
Buscher K., Marcovecchio P., Hedrick C.C., Ley K. Patrolling Mechanics of Non-Classical Monocytes in Vascular Inflammation. Front. Cardiovasc. Med., 2017, Vol. 4, pp. 80.	
doi: 10.3389/fcvm.2017.00080	

5	
	
Cranford T.L., Velázquez K.T., Enos R.T., Bader J.E., Carson M.S., Chatzistamou I., Nagarkatti M., Murphy E.A. Loss of monocyte chemoattractant protein-1 expression delays mammary tumorigenesis and reduces localized inflammation in the C3(1)/SV40Tag triple negative breast cancer model. Cancer Biol. Ther., 2017, Vol. 18, no. 2, pp. 85-93.	
doi: 10.1080/15384047.
2016.1276135	

6	
	
Fridman W.H. From Cancer Immune Surveillance to Cancer Immunoediting: Birth of Modern Immuno-Oncology. J. Immunol., 2018, Vol. 201, no. 3, pp. 825-826.	
doi: 10.4049/jimmunol.
1800827	

7	
	
Gordon S. Targeting a monocyte subset to reduce inflammation. Circ. Res., 2012, Vol. 110, no. 12, pp. 1546-1548.	
doi: 10.1161/RES.
0b013e31825ec26d	

8	
	
Jan H.C., Yang W.H., Ou C.H. Combination of the Preoperative Systemic Immune-Inflammation Index and Monocyte-Lymphocyte Ratio as a Novel Prognostic Factor in Patients with Upper-Tract Urothelial Carcinoma. Ann. Surg. Oncol., 2019, Vol. 26, no. 2, pp. 669-684.	
doi: 10.1245/s10434-018-6942-3	

9	
	
Jones M.B., Alvarez C.A., Johnson J.L., Zhou J.Y., Morris N., Cobb B.A. CD45Rb-low effector T cells require IL-4 to induce IL-10 in FoxP3 Tregs and to protect mice from inflammation. PLoS One, 2019, Vol. 14, no. 5, e0216893.	
doi: 10.1371/journal.
pone.0216893	

10	
	
Juhas U., Ryba-Stanisławowska M., Brandt-Varma A., Myśliwiec M., Myśliwska J. Monocytes of newly diagnosed juvenile DM1 patients are prone to differentiate into regulatory IL-10(+) M2 macrophages. Immunol. Res., 2019, Vol. 67, no. 1, pp. 58-69.	
doi: 10.1007/s12026-019-09072-0	

11	
	
Komala A.S., Rachman A. Association of Peripheral Monocyte Count with Soluble P-Selectin and Advanced Stages in Nasopharyngeal Carcinoma. Adv. Hematol., 2018, 2018:3864398.	
doi: 10.1155/2018/3864398	

12	
	
Komura T., Sakai Y., Harada K., Kawaguchi K., Takabatake H., Kitagawa H., Wada T., Honda M., Ohta T., Nakanuma Y., Kaneko S. Inflammatory features of pancreatic cancer highlighted by monocytes/macrophages and CD4+ T cells with clinical impact. Cancer Sci., 2015, Vol. 106, no. 6, pp. 672-686.	
doi: 10.1111/cas.12663	

13	
	
Kong B.S., Kim Y., Kim G.Y., Hyun J.W., Kim S.H., Jeong A., Kim H.J. Increased frequency of IL-6-producing non-classical monocytes in neuromyelitis optica spectrum disorder. J. Neuroinflammation, 2017, Vol. 14, no. 1, pp. 191.	
doi: 10.1186/s12974-017-0961-z	

14	
Кудрявцев И.В., Субботовская А.И. Опыт измерения параметров иммунного статуса с использованием шести-цветного цитофлуоримерического анализа // Медицинская иммунология.–2015.–Т. 17, № 1.–С. 19-26.	
Kudryavtsev I.V., Subbotovskaya A.I. Application of six-color flow cytometric analysis for immune profile monitoring. Medical Immunology, 2015, Vol. 17, no. 1, pp. 19-26.	
https://doi.org/10.15789/
1563-0625-2015-1-19-26	

15	
	
Li X., Chen Y., Liu X., Zhang J., He X., Teng G., Yu D. Tim3/Gal9 interactions between T cells and monocytes result in an immunosuppressive feedback loop that inhibits Th1 responses in osteosarcoma patients. Int. Immunopharmacol., 2017, Vol. 44, pp. 153-159.	
doi: 10.1016/j.intimp.
2017.01.006	

16	
	
Maecker H., McCoy P., Nussenblatt R. Standardizing immunophenotyping for the human immunology project. Nat. Rev. Immunol., 2012, Vol. 12, pp. 191-200.	
DOI: 10.1038/nri3158	

17	
	
Mahmoodpoor A., Paknezhad S., Shadvar K., Hamishehkar H., Movassaghpour A.A., Sanaie S., Ghamari A.A., Soleimanpour H. Flow Cytometry of CD64, HLA-DR, CD25, and TLRs for Diagnosis and Prognosis of Sepsis in Critically Ill Patients Admitted to the Intensive Care Unit: A Review Article. Anesth. Pain Med., 2018, Vol. 8, no. 6, e83128.	
doi: 10.5812/aapm.83128	

18	
	
Moreau R., Périanin A., Arroyo V. Review of Defective NADPH Oxidase Activity and Myeloperoxidase Release in Neutrophils From Patients With Cirrhosis. Front. Immunol., 2019, Vol. 10, pp. 1044.	
doi: 10.3389/fimmu.
2019.01044	

19	
	
Mukherjee R., Kanti Barman P., Kumar Thatoi P., Tripathy R., Kumar Das B., Ravindran B. Non-Classical monocytes display inflammatory features: Validation in Sepsis and Systemic Lupus Erythematous. Sci. Rep., 2015, Vol. 5, pp. 13886.	
doi: 10.1038/srep13886	

20	
	
Naranjo-Gómez J.S., Castillo J.A., Rojas M., Restrepo B.N., Diaz F.J., Velilla P.A., Castaño D. Different phenotypes of non-classical monocytes associated with systemic inflammation, endothelial alteration and hepatic compromise in patients with dengue. Immunology, 2019, Vol. 156, no. 2, pp. 147-163.	
doi: 10.1111/imm.13011	

21	
	
Narasimhan P.B., Marcovecchio P., Hamers A.A.J., Hedrick C.C. Nonclassical Monocytes in Health and Disease. Annu. Rev. Immunol., 2019, Vol. 37, pp. 439-456.	
doi: 10.1146/annurev-immunol-042617-053119	

22	
	
O'Donnell J.S., Teng M.W.L., Smyth M.J. Cancer immunoediting and resistance to T cell-based immunotherapy. Nat. Rev. Clin. Oncol., 2019, Vol. 16, no. 3, pp. 151-167.	
doi: 10.1038/s41571-018-0142-8	

23	
	
Pence B.D., Yarbro J.R. Classical monocytes maintain ex vivo glycolytic metabolism and early but not later inflammatory responses in older adults. Immun. Ageing, 2019, Vol. 16, pp. 3.	
doi: 10.1186/s12979-019-0143-1	

24	
	
Pohar J., Simon Q., Fillatreau S. Antigen-Specificity in the Thymic Development and Peripheral Activity of CD4(+)FOXP3(+) T Regulatory Cells. Front. Immunol., 2018, Vol. 9, pp. 1701.	
doi: 10.3389/fimmu.
2018.01701	

25	
	
Ramello M.C., Tosello Boari J., Canale F.P., Mena H.A., Negrotto S., Gastman B., Gruppi A., Acosta Rodríguez E.V., Montes C.L. Tumor-induced senescent T cells promote the secretion of pro-inflammatory cytokines and angiogenic factors by human monocytes/macrophages through a mechanism that involves Tim-3 and CD40L. Cell Death Dis., 2014, Vol. 5, e1507.	
doi: 10.1038/cddis.2014.451	

26	
	
Romano E., Kusio-Kobialka M., Foukas P.G., Baumgaertner P., Meyer C., Ballabeni P., Michielin O., Weide B., Romero P., Speiser D.E. Ipilimumab-dependent cell-mediated cytotoxicity of regulatory T cells ex vivo by nonclassical monocytes in melanoma patients. Proc. Natl. Acad. Sci. USA, 2015, Vol. 112, no. 19, pp. 6140-6145.	
doi: 10.1073/pnas.1417320112	

27	
	
Sabir F., Farooq R.K., Asim Ur. Rehman, Ahmed N. Monocyte as an Emerging Tool for Targeted Drug Delivery: A Review. Curr. Pharm. Des., 2018, Vol. 24, no. 44, pp. 5296-5312.	
doi: 10.2174/
1381612825666190102104642	

28	
	
Salminen A., Kauppinen A., Kaarniranta K. Myeloid-derived suppressor cells (MDSC): an important partner in cellular/tissue senescence. Biogerontology, 2018, Vol. 19, no. 5, pp. 325-339.	
doi: 10.1007/s10522-018-9762-8	

29	
Савченко А.А., Борисов А.Г., Модестов А.А., Мошев А.В., Кудрявцев И.В., Тоначева О.Г., Кощеев В.Н. Фенотипический состав и хемилюминесцентная активность моноцитов у больных почечно-клеточным раком // Медицинская иммунология.2015.Т. 17, № 2.С. 141-150.	
Savchenko A.A., Borisov A.G., Modestov A.A., Moshev A.V., Kudryavtsev I.V., Tonacheva O.G., Koshcheev V.N. Monocytes subpopulations and chemiluminescent activity in patients with renal cell carcinoma. Medical Immunology, 2015, Vol. 17, no. 2, pp. 141-150.	
https://doi.org/10.15789/1563-0625-2015-2-141-150	

30	
Савченко А.А., Кудрявцев И.В., Борисов А.Г. Методы оценки и роль респираторного взрыва в патогенезе инфекционно-воспалительных заболеваний // Инфекция и иммунитет.2017.Т. 7б № 4.С. 327-340.	
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https://doi.org/10.15789/2220-7619-2017-4-327-340	

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Shevach E.M. Foxp3(+) T Regulatory Cells: Still Many Unanswered Questions-A Perspective After 20 Years of Study. Front. Immunol., 2018, Vol. 9, pp. 1048.	
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Stansfield B.K., Ingram D.A. Clinical significance of monocyte heterogeneity. Clin. Transl. Med., 2015, Vol. 4, pp. 5.	
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van de Geer A., Cuadrado E., Slot M.C., van Bruggen R., Amsen D., Kuijpers T.W. Regulatory T cell features in chronic granulomatous disease. Clin. Exp. Immunol., 2019, Vol. 197, no. 2, pp. 222-229.	
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Wagner M., Koyasu S. Cancer Immunoediting by Innate Lymphoid Cells. Trends Immunol., 2019, Vol. 40, no. 5, pp. 415-430.	
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Wouters K., Gaens K., Bijnen M., Verboven K., Jocken J., Wetzels S., Wijnands E., Hansen D., van Greevenbroek M., Duijvestijn A., Biessen E.A., Blaak E.E., Stehouwer C.D., Schalkwijk C.G. Circulating classical monocytes are associated with CD11c(+) macrophages in human visceral adipose tissue. Sci. Rep., 2017, Vol. 7, pp. 42665.	
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Yu C.X., Bai L.Y., Lin J.J., Li S.B., Chen J.Y., He W.J., Yu X.M., Cui X.P., Wang H.L., Chen Y.Z., Zhu L. rhPLD2 inhibits airway inflammation in an asthmatic murine model through induction of stable CD25(+) Foxp3(+) Tregs. Mol. Immunol., 2018, Vol. 101, pp. 539-549.	
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39	
	
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Zhuang Y., Peng H., Chen Y., Zhou S., Chen Y. Dynamic monitoring of monocyte HLA-DR expression for the diagnosis, prognosis, and prediction of sepsis. Front. Biosci. (Landmark Ed), 2017, Vol. 22, pp. 1344-1354.	
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