ROLE OF DIFFERENT B CELL SUBPOPULATIONS IN IMMUNE RESPONSE TO T-INDEPENDENT TYPE 2 ANTIGENS
https://doi.org/10.15789/1563-0625-2007-1-39-46
Abstract
Abstract. The role of different B-cell subpopulations in polyclonal B-cell activation induced by T-independent antigens type 2 (TI-2) was under studies. CD5+B/B-1 cells were isolated from the spleens of mice immunized with polyvinyl pirrolidone, or á(1→3) dextran. The numbers of antibody (Ab) and Ig-producers in CD5+B/B-1 splenocytes were determined by ELISPOT. The number of cells producing unspecific Ig was calculated as a difference between the numbers of Ig- and Ab-producers; the numbers of nonspecific Ig-producing splenocytes induced by TI-2 immunization were determined as differences between their contents in immunized and control animals. In experiments with CD5+ and CD5– splenocytic populations, the development of Ab-producers and increased numbers of cells producing unspecific Ig was dependent on the CD5+ B-cells. These data were confirmed in experiments with subpopulations of B-1 and B-2 lymphocytes obtained with Dynal separation kit. In spite of sufficient predominance of B-cells in B-2 fraction (91% vs ~13% in B-1 fraction), the numbers of Ab and TI-2-induced nonspecific Ig-producers were nearly similar for the both cell fractions. Taking into account relative contents of B-cells, the numbers of Aband unspecific Ig- producers in B-1 fraction were 6- to 7-fold higher than in B-2 fraction. Thus, dependence on the B-1 cells exists both for polyclonal immune reactions to polyvinylpirrolidone and dextran, and specific response. Simultaneous injection of two TI-2 antigens did not induce additive effects upon the numbers of unspecific Ig-producers in B-1 fraction, in spite of marked increase in amounts of these cells after separate immunization with either of these antigens. It is concluded that polyclonal activation of B-1 cells by TI-2 antigens is subject to restriction which may depend either on the size of B-cell pool available for activation, or on insufficiency of appropriate stimulating factors.
About the Authors
M. V. GavrilovaRussian Federation
I. N. Chernyshova
Russian Federation
E. V. Sidorova
Russian Federation
References
1. Агаджанян М.Г., Меграбян Т.Б., Сидорова Е.В. Нарастание числа клеток, секретирующих антитела и клеток, секретирующих неспецифические иммуноглобулины, при иммунизации мышей Т-зависимым и Т-независимым антигенами // Бюлл. эксперим. биол. мед. – 1981. – Т. 92. – С. 66-68.
2. Агаджанян М.Г., Смирнова И.Н.,Сидорова Е.В. Зависимость образования продуцентов антигензависимых неспецифических иммуноглобулинов от дозы Т-зависимого и Т-независимых антигенов // Бюлл. эксперим. биол. мед. – 1986. – Т. СII – № 8. – С. 206-208.
3. Сидорова Е.В. Что нам известно сегодня о В-клетках // Успехи современ. биологии. – 2006. – Т. 126. – № 3. – С. 227-242.
4. Bakay M., Biladi I., Berencsi K., Sidorova E., Agadzhanian M., Fachet F., Erdei J. Immunoenhancement and suppression induced by adenovirus in chicken // Acta Virol. – 1992. – Vol. 36. – Р. 269-276.
5. Baumgarth N., Tung J.W., Herzenberg L.A. Inherent specificities in natural antibodies: a key to immune defense against pathogen invasion // Springer Semin. Immun. – 2005. – Vol. 26. – P. 347-362.
6. Boyd W.C., Bernard H. Quantitative changes in antibodies and -globulin fraction in sera of rabbits injected with several antigens // J. Immunol. – 1937. – V. 33. – P. 111-122.
7. Chandrashekhar P., Medzhitov R. Control of B-cell responses by Toll-like receptors // Nature Letters – 2005. – Vol. 438. – P. 364-368.
8. Hardy R.R., Hayakawa K. B cell development pathways // Ann. Rev. Immunol. – 2001. – Vol. 19. – P. 595-621.
9. Martin F., Kearney J. B-cell subsets and the mature preimmune repertoire. Marginal zone and 1 cells as part of a «natural immune memory» // Immunol. Rev. – 2000. – Vol. 175. – P. 70-79.
10. Mond J.J, Lees A., Snapper C.M. T cellindependent antigens type 2 // Ann. Rev. Immunol. – 1995. – V. 13. – P. 655-692.
11. Oliver A.M, Martin F., Gartland G.L., Carter R.H., Kearney J.F. Marginal zone B cells exhibit unique activation, proliferative and immunoglobulin secretory responses // Eur. J. Immunol. – 1997. – Vol. 27, N 7. – P. 2366-2374.
12. Pers J.O., Jamin C.,Youinou P., Charreire J. Role of IL-10 in the distribution of B cell subsets in the mouse B-1 cellpopulation // Eur. Cytokine Netw. – 2003. – Vol. 14, N 3 – P. 178-185.
13. Seman M., Mazie J.C., Bussard A.E. Antigenic properties of a water soluble fraction of sheep erythrocytes // Eur. J. Immunol. – 1972. – Vol. 4. – P. 387-388.
14. Sidorova E.V, Agadzhanian M.G., Mazhul L.A., Biladi I., Bakai M., Berenchi K. Immunosuppresson induced by respiratory viruses (influenza virus, adenovirus) in mice // Biull. Eksp. Biol. Med. – 1991. – Vol. 111. – P. 510-512.
15. Sidorova E.V., Li-Sheng Lu, Devlin B., Chernishova I., Gavrilova M. Role of different B-cell subsets in the specific and polyclonal immune response to T-independent antigens type 2 // Immunol. Letts. – 2003. – Vol. 88. – P. 37-42.
16. Wells S.M., Kantor A.B., Stall A.M. CD43(S7) expression identifies peripheral B cell subsets // J. Immunol. – 1994. – Vol. 153, N 12. – P. 5503- 5515.
Review
For citations:
Gavrilova M.V., Chernyshova I.N., Sidorova E.V. ROLE OF DIFFERENT B CELL SUBPOPULATIONS IN IMMUNE RESPONSE TO T-INDEPENDENT TYPE 2 ANTIGENS. Medical Immunology (Russia). 2007;9(1):39-46. (In Russ.) https://doi.org/10.15789/1563-0625-2007-1-39-46