IgM- and IgA-response of peritoneal B-1 cells to the TI-2 antigen with the presence of γδT cells in vitro

IgA is an important component of the mucosal system of the body. It limits penetration of pathogens into the bloodstream. Inflammatory diseases such as Crohn disease and colitis may be associated with disorders of IgA synthesis. Both B1 and B2 cells are a source of IgA in the intestines. Special att...

Full description

Bibliographic Details
Main Authors: N. A. Snegireva, E. V. Sidorova, I. N. Dyakov, M. V. Gavrilova, I. N. Chernyshova, E. P. Pashkov, O. A. Svitich
Format: Article
Language:Russian
Published: St. Petersburg branch of the Russian Association of Allergologists and Clinical Immunologists 2021-05-01
Series:Медицинская иммунология
Subjects:
Online Access:https://www.mimmun.ru/mimmun/article/view/2157
_version_ 1797197891178070016
author N. A. Snegireva
E. V. Sidorova
I. N. Dyakov
M. V. Gavrilova
I. N. Chernyshova
E. P. Pashkov
O. A. Svitich
author_facet N. A. Snegireva
E. V. Sidorova
I. N. Dyakov
M. V. Gavrilova
I. N. Chernyshova
E. P. Pashkov
O. A. Svitich
author_sort N. A. Snegireva
collection DOAJ
description IgA is an important component of the mucosal system of the body. It limits penetration of pathogens into the bloodstream. Inflammatory diseases such as Crohn disease and colitis may be associated with disorders of IgA synthesis. Both B1 and B2 cells are a source of IgA in the intestines. Special attention is paid to B1 cells, which are able to respond to T-independent type 2 antigens and produce natural antibodies. B1 cells produce about 50% of the intestinal IgA including specific antibodies to the components of microorganisms contained in the gastrointestinal tract. The mechanism of IgA formation in the T-independent way is not investigated in details. It was suggested that the γδТ-cells promote switching to IgA synthesis by B1 cells. This assumption may be supported by their co-localization with B1 lymphocytes in the intestinal mucosa, as well as participation, along with B1 cells, in formation of the first-line defense against the pathogens. In addition, the both lymphocyte subpopulations evolve during initial ontogenesis, earlier than “classic” В2 and αβT cells. Therefore, it was suggested that γδT lymphocytes may be involved into the processes of induction and/or regulation of IgM and IgA production by B1 cells in response to TH2 antigens.In the present study, we have shown the effect of γδT cells upon generation of IgM- and IgA-forming B1 cells in response to α-1,3-dextran in vitro. We also studied the dynamics of the mRNA expression for IgM- and IgA-heavy chains by the B1 cells at different terms of in vitro culture.It was found that, during co-cultivation of B1 cells with 20% γδT lymphocytes, there is no increase in the number of dextran-specific IgM-producing cells. The B1 cells exhibited an increase of IgM heavy chain mRNA expression in response to dextran but not in co-cultures. Expression of mRNA for IgM heavy chains in co-cultures was decreased compared to non-treated B-cell cultures. Contrary to the earlier assumption, a presence of γδT lymphocytes in culture did not enhance the formation of IgA producents. The obtained data suggest regulatory properties of the γδТ lymphocytes during the B1 cells response to T-independent antigens.
first_indexed 2024-03-08T05:47:47Z
format Article
id doaj.art-6fa2a1a611a6469b960b0a597eeca8cb
institution Directory Open Access Journal
issn 1563-0625
2313-741X
language Russian
last_indexed 2024-04-24T06:51:10Z
publishDate 2021-05-01
publisher St. Petersburg branch of the Russian Association of Allergologists and Clinical Immunologists
record_format Article
series Медицинская иммунология
spelling doaj.art-6fa2a1a611a6469b960b0a597eeca8cb2024-04-22T13:07:46ZrusSt. Petersburg branch of the Russian Association of Allergologists and Clinical ImmunologistsМедицинская иммунология1563-06252313-741X2021-05-0123224525610.15789/1563-0625-IAI-21571393IgM- and IgA-response of peritoneal B-1 cells to the TI-2 antigen with the presence of γδT cells in vitroN. A. Snegireva0E. V. Sidorova1I. N. Dyakov2M. V. Gavrilova3I. N. Chernyshova4E. P. Pashkov5O. A. Svitich6I. Mechnikov Research Institute for Vaccines and SeraI. Mechnikov Research Institute for Vaccines and SeraI. Mechnikov Research Institute for Vaccines and SeraI. Mechnikov Research Institute for Vaccines and SeraI. Mechnikov Research Institute for Vaccines and SeraI. Sechenov First Moscow State Medical UniversityI. Mechnikov Research Institute for Vaccines and Sera; I. Sechenov First Moscow State Medical UniversityIgA is an important component of the mucosal system of the body. It limits penetration of pathogens into the bloodstream. Inflammatory diseases such as Crohn disease and colitis may be associated with disorders of IgA synthesis. Both B1 and B2 cells are a source of IgA in the intestines. Special attention is paid to B1 cells, which are able to respond to T-independent type 2 antigens and produce natural antibodies. B1 cells produce about 50% of the intestinal IgA including specific antibodies to the components of microorganisms contained in the gastrointestinal tract. The mechanism of IgA formation in the T-independent way is not investigated in details. It was suggested that the γδТ-cells promote switching to IgA synthesis by B1 cells. This assumption may be supported by their co-localization with B1 lymphocytes in the intestinal mucosa, as well as participation, along with B1 cells, in formation of the first-line defense against the pathogens. In addition, the both lymphocyte subpopulations evolve during initial ontogenesis, earlier than “classic” В2 and αβT cells. Therefore, it was suggested that γδT lymphocytes may be involved into the processes of induction and/or regulation of IgM and IgA production by B1 cells in response to TH2 antigens.In the present study, we have shown the effect of γδT cells upon generation of IgM- and IgA-forming B1 cells in response to α-1,3-dextran in vitro. We also studied the dynamics of the mRNA expression for IgM- and IgA-heavy chains by the B1 cells at different terms of in vitro culture.It was found that, during co-cultivation of B1 cells with 20% γδT lymphocytes, there is no increase in the number of dextran-specific IgM-producing cells. The B1 cells exhibited an increase of IgM heavy chain mRNA expression in response to dextran but not in co-cultures. Expression of mRNA for IgM heavy chains in co-cultures was decreased compared to non-treated B-cell cultures. Contrary to the earlier assumption, a presence of γδT lymphocytes in culture did not enhance the formation of IgA producents. The obtained data suggest regulatory properties of the γδТ lymphocytes during the B1 cells response to T-independent antigens.https://www.mimmun.ru/mimmun/article/view/2157igmigab-1 cellsγδt cellsti-2 antigenintestinedextran
spellingShingle N. A. Snegireva
E. V. Sidorova
I. N. Dyakov
M. V. Gavrilova
I. N. Chernyshova
E. P. Pashkov
O. A. Svitich
IgM- and IgA-response of peritoneal B-1 cells to the TI-2 antigen with the presence of γδT cells in vitro
Медицинская иммунология
igm
iga
b-1 cells
γδt cells
ti-2 antigen
intestine
dextran
title IgM- and IgA-response of peritoneal B-1 cells to the TI-2 antigen with the presence of γδT cells in vitro
title_full IgM- and IgA-response of peritoneal B-1 cells to the TI-2 antigen with the presence of γδT cells in vitro
title_fullStr IgM- and IgA-response of peritoneal B-1 cells to the TI-2 antigen with the presence of γδT cells in vitro
title_full_unstemmed IgM- and IgA-response of peritoneal B-1 cells to the TI-2 antigen with the presence of γδT cells in vitro
title_short IgM- and IgA-response of peritoneal B-1 cells to the TI-2 antigen with the presence of γδT cells in vitro
title_sort igm and iga response of peritoneal b 1 cells to the ti 2 antigen with the presence of γδt cells in vitro
topic igm
iga
b-1 cells
γδt cells
ti-2 antigen
intestine
dextran
url https://www.mimmun.ru/mimmun/article/view/2157
work_keys_str_mv AT nasnegireva igmandigaresponseofperitonealb1cellstotheti2antigenwiththepresenceofgdtcellsinvitro
AT evsidorova igmandigaresponseofperitonealb1cellstotheti2antigenwiththepresenceofgdtcellsinvitro
AT indyakov igmandigaresponseofperitonealb1cellstotheti2antigenwiththepresenceofgdtcellsinvitro
AT mvgavrilova igmandigaresponseofperitonealb1cellstotheti2antigenwiththepresenceofgdtcellsinvitro
AT inchernyshova igmandigaresponseofperitonealb1cellstotheti2antigenwiththepresenceofgdtcellsinvitro
AT eppashkov igmandigaresponseofperitonealb1cellstotheti2antigenwiththepresenceofgdtcellsinvitro
AT oasvitich igmandigaresponseofperitonealb1cellstotheti2antigenwiththepresenceofgdtcellsinvitro