Инфекция и иммунитет. 2015; 5: 63-70
СОСТОЯНИЕ КЛЕТОЧНОГО И ГУМОРАЛЬНОГО ИММУНИТЕТА В ЗАВИСИМОСТИ ОТ ИСХОДА РАСПРОСТРАНЕННОГО ГНОЙНОГО ПЕРИТОНИТА
Савченко А. А., Борисов А. Г., Здзитовецкий Д. Э., Кудрявцев И. В.
https://doi.org/10.15789/2220-7619-2015-1-63-70Аннотация
Целью исследования явилось изучение состояния клеточного и гуморального иммунитета у больных с распространенным гнойным перитонитом (РГП) в зависимости от исхода заболевания. Обследовано 50 больных РГП внебольничного и госпитального происхождения. Исследование фенотипа лимфоцитов крови проводили методом проточной цитометрии. Концентрацию иммуноглобулинов и цитокинов определяли иммуноферментным методом. Установлено, что состояние иммунной системы при РГП характеризуется лейкоцитозом, относительной лимфопенией, увеличением концентрации провоспалительных цитокинов, а также снижением содержания цитотоксических и активированных Т-лимфоцитов. Состояние клеточного звена иммунной системы при неблагоприятном исходе РГП характеризуется снижением уровней γδТ-лимфоцитов и NKT-клеток при повышении количества В1-лимфоцитов. Состояние иммунной системы при благоприятном исходе РГП характеризуется снижением количества NK-клеток в периферической крови и повышением содержания Th2-лимфоцитов. Увеличение количества Th2-клеток определяет усиление стимулирующего влияния Т-клеточного звена на гуморальный иммунитет, что проявляется в увеличении концентраций IL-4 и IgA, что и является важным фактором в иммунопатогенезе РГП, определяющим его благоприятный исход.
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Russian Journal of Infection and Immunity. 2015; 5: 63-70
THE CELLULAR AND HUMORAL IMMUNITY STATE DEPENDING ON THE OUTCOME OF A WIDESPREAD PURULENT PERITONITIS
Savchenko A. A., Borisov A. G., Zdzitoveckij D. E., Kudryavtsev I. V.
https://doi.org/10.15789/2220-7619-2015-1-63-70Abstract
The aim of the study was to examine the state of cellular and humoral immunity in patients with widespread purulent peritonitis (WPP) in depending on the disease outcome. The study involved 50 patients with community-acquired and hospital origin WPP. The testing of blood lymphocyte phenotype was performed by flow cytometry. The concentration of immunoglobulins and cytokines were measured by ELISA. It was established that the immune system state by WPP is characterized by leukocytosis, relative lymphopenia, increasing concentrations of pro-inflammatory cytokines, as well as decrease of the cytotoxic and activated T-lymphocytes content. The state of the cellular immunity in case of unfavorable outcome of the WPP is characterized by decreased of the γδT-lymphocytes and NKT-cells levels with increasing amounts of the B1-cells. The immune system state in case of a favorable outcome of the WPP is characterized by a decrease in the number of NK-cells in peripheral blood and increased levels of Th2-lymphocytes. Increasing of the Th2-cells number determines the increase in stimulating effects of T-cell on the humoral immunity, that is manifested in increasing concentrations of IL-4 and IgA, which is an important factor in the immunopathogenesis of the WPP determining its favorable outcome.
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12. Griffin D.O., Rothstein T.L. Human B1 cell frequency: isolation and analysis of human B1 cells. Front. Immunol., 2012, vol. 3, pp. 122–123.
13. Griveas I., Fleva A., Karanikas E., Gogos K., Sakellariou G. CD4/CD8 T-cell ratio in peritoneal dialysis effluents predicts the outcome of peritonitis in patients undergoing continuous ambulatory peritoneal dialysis. Artif. Organs., 2009, vol. 33, no. 12, pp. 1091–1095.
14. Harris N., Gause W.C. To B or not to B: B cells and the Th2-type immune response to helminthes. Trends Immunol., 2011, vol. 32, no. 2, pp. 80–88.
15. KiankC.,EntleutnerM.,FürllB.,WesterholtA.,HeideckeC.D.,SchüttC.Stress-inducedimmuneconditioningaffectsthecourse of experimental peritonitis. Shock, 2007, vol. 27, no. 3, pp. 305–311.
16. Kleinnijenhuis J., Quintin J., Preijers F., Joosten L.A., Jacobs C., Xavier R.J., Van Der Meer J.W., Van Crevel R., Netea M.G. BCG-induced trained immunity in NK cells: role for non-specific protection to infection. Clin. Immunol., 2014, vol. 155, no. 2, pp. 213–219.
17. Le Gall J.-R., Lemeshow S., Saulnier F. A new simplified acute physiology score (SAPS II) based on a European/North American multicenter study. JAMA, 1993, vol. 270, pp. 2957–2963.
18. Lertworapreecha M., Patumraj S., Niruthisard S., Hansasuta P., Bhattarakosol P. Cytotoxic function of gamma delta (gamma/ delta) T cells against pamidronate-treated cervical cancer cells. Indian J. Exp. Biol., 2013, vol. 51, no. 8, pp. 597–605.
19. Linder M.M., Wacha H., Feldmann U., Wesch G., Streifensand R.A., Gundlach E. Der Mannheimer Peritonitis-Index. Ein Instrument zur intraoperativen Prognose der Peritonitis. Chirurg, 1987, no. 58, pp. 84–91.
20. Luider J., Cyfra M., Johnson P., Auer I. Impact of the new Beckman Coulter Cytomics FC 500 5-color flow cytometer on a regional flow cytometry clinical laboratory service. Lab. Hematol., 2004, vol. 10, pp. 102–108.
21. Maecker H., McCoy P., Nussenblatt R. Standardizing immunophenotyping for the human immunology project. Nat. Rev. Immunol., 2012, vol. 12, pp. 191–200.
22. MarçaisA.,WalzerT.mTOR:agatetoNKcellmaturationandactivation.CellCycle,2014,vol.13,no.21,pp.3315–3316.
23. McKee S.J., Mattarollo S.R., Leggatt G.R. Immunosuppressive roles of natural killer T (NKT) cells in the skin. J. Leukoc. Biol., 2014, vol. 96, no. 1, pp. 49–54.
24. 24. PillaiM.R.,BixM.EvolutionofIL4andpathogenantagonism.GrowthFactors,2011,vol.29,no.4,pp.153–160.
25. SistaF.,SchietromaM.,SantisG.D.,MatteiA.,CeciliaE.M.,PiccioneF.,LeardiS.,CarleiF.,AmicucciG.Systemicinflammation and immune response after laparotomy vs laparoscopy in patients with acute cholecystitis, complicated by peritonitis. World J. Gastrointest. Surg., 2013, vol. 5, no. 4, pp. 73–82.
26. Terabe M., Berzofsky J.A. The immunoregulatory role of type I and type II NKT cells in cancer and other diseases. Cancer Immunol. Immunother., 2014, vol. 63, no. 3, pp. 199–213.
27. VasudevA.,YingC.T.,AyyadhuryS.,PuanK.J.,AndiappanA.K.,NyuntM.S.,ShadanN.B.,MustafaS.,LowI.,RotzschkeO., Fulop T., Ng T.P., Larbi A. γ/δ T cell subsets in human aging using the classical α/β T cell model. J. Leukoc. Biol., 2014, vol. 96, no. 4, pp. 647–655.
28. VincentJ.L.,MorenoR.,TakalaJ.,WillattsS.,DeMendonçaA.,BruiningH.,ReinhartC.K.,SuterP.M.,ThijsL.G.TheSOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on SepsisRelated Problems of the European Society of Intensive Care Medicine. Intensive Care Med., 1996, vol. 22, no. 7, pp. 707–710.
29. WiestR.,KragA.,GerbesA.Spontaneousbacterialperitonitis:recentguidelinesandbeyond.Gut,2012,vol.61,no.2,pp.297–310.
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