How to B(e)-1 Important Cell During Leishmania Infection
B-1 cells are an innate-like population of B lymphocytes that are subdivided into B-1a and B-1b distinguished by the presence or absence of CD5, respectively. B-1 cells can act as regulatory B cells, are able to present antigen and produce IL-10. Leishmaniasis in humans is a complex of diseases caus...
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Published in | Frontiers in cellular and infection microbiology Vol. 9; p. 424 |
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Main Authors | , , , , , |
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Language | English |
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Abstract | B-1 cells are an innate-like population of B lymphocytes that are subdivided into B-1a and B-1b distinguished by the presence or absence of CD5, respectively. B-1 cells can act as regulatory B cells, are able to present antigen and produce IL-10. Leishmaniasis in humans is a complex of diseases caused by parasites of the genus
. More than 20 species can infect humans, with each species causing the development of different immunological responses in the host. Susceptibility is usually related to the production of anti-inflammatory cytokines while the production of Th1 cytokines is indicative of resistance. However, few studies have attempted to evaluate the role of B-1 cells during either the
infection or
interaction with
parasites.
studies were performed using XID mice model, BALB/Xid mice have a mutation in the Bruton's tyrosine kinase, which is an important enzyme for developing B-1 and maturing B-2 lymphocytes leading to the presence of immature B-2 cells. Here, we compile these studies and assess the influence of B-1 cells on disease progression with different
species. |
---|---|
AbstractList | B-1 cells are an innate-like population of B lymphocytes that are subdivided into B-1a and B-1b distinguished by the presence or absence of CD5, respectively. B-1 cells can act as regulatory B cells, are able to present antigen and produce IL-10. Leishmaniasis in humans is a complex of diseases caused by parasites of the genus
. More than 20 species can infect humans, with each species causing the development of different immunological responses in the host. Susceptibility is usually related to the production of anti-inflammatory cytokines while the production of Th1 cytokines is indicative of resistance. However, few studies have attempted to evaluate the role of B-1 cells during either the
infection or
interaction with
parasites.
studies were performed using XID mice model, BALB/Xid mice have a mutation in the Bruton's tyrosine kinase, which is an important enzyme for developing B-1 and maturing B-2 lymphocytes leading to the presence of immature B-2 cells. Here, we compile these studies and assess the influence of B-1 cells on disease progression with different
species. B-1 cells are an innate-like population of B lymphocytes that are subdivided into B-1a and B-1b distinguished by the presence or absence of CD5, respectively. B-1 cells can act as regulatory B cells, are able to present antigen and produce IL-10. Leishmaniasis in humans is a complex of diseases caused by parasites of the genus Leishmania. More than 20 species can infect humans, with each species causing the development of different immunological responses in the host. Susceptibility is usually related to the production of anti-inflammatory cytokines while the production of Th1 cytokines is indicative of resistance. However, few studies have attempted to evaluate the role of B-1 cells during either the in vivo infection or in vitro interaction with Leishmania parasites. In vivo studies were performed using XID mice model, BALB/Xid mice have a mutation in the Bruton's tyrosine kinase, which is an important enzyme for developing B-1 and maturing B-2 lymphocytes leading to the presence of immature B-2 cells. Here, we compile these studies and assess the influence of B-1 cells on disease progression with different Leishmania species. B-1 cells are an innate-like population of B lymphocytes that are subdivided into B-1a and B-1b distinguished by the presence or absence of CD5, respectively. B-1 cells can act as regulatory B cells, are able to present antigen and produce IL-10. Leishmaniasis in humans is a complex of diseases caused by parasites of the genus Leishmania . More than 20 species can infect humans, with each species causing the development of different immunological responses in the host. Susceptibility is usually related to the production of anti-inflammatory cytokines while the production of Th1 cytokines is indicative of resistance. However, few studies have attempted to evaluate the role of B-1 cells during either the in vivo infection or in vitro interaction with Leishmania parasites. In vivo studies were performed using XID mice model, BALB/Xid mice have a mutation in the Bruton's tyrosine kinase, which is an important enzyme for developing B-1 and maturing B-2 lymphocytes leading to the presence of immature B-2 cells. Here, we compile these studies and assess the influence of B-1 cells on disease progression with different Leishmania species. |
Author | Firmino-Cruz, Luan Morrot, Alexandre de Matos Guedes, Herbert Leonel Decote-Ricardo, Debora Gomes, Daniel Claudio de Oliveira Freire-de-Lima, Celio Geraldo |
AuthorAffiliation | 7 Laboratório de Imunomodulação, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal Do Rio de Janeiro , Rio de Janeiro , Brazil 8 Núcleo Multidisciplinar de Pesquisa UFRJ—Xerém em Biologia (NUMPEX-BIO), UFRJ Campus Duque de Caxias Professor Geraldo Cidade, Universidade Federal Do Rio de Janeiro , Duque de Caxias , Brazil 2 Laboratório Interdisciplinar de Pesquisas Médicas, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz , Rio de Janeiro , Brazil 5 Laboratório de Imunopatologia, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz , Rio de Janeiro , Brazil 4 Núcleo de Doenças Infecciosas/Núcleo de Biotecnologia, Universidade Federal Do Espírito Santo , Vitoria , Brazil 6 Faculdade de Medicina, Universidade Federal Do Rio de Janeiro , Rio de Janeiro , Brazil 3 Instituto de Veterinária, Universidade Federal Rural Do Rio de Janeiro , Seropédica , Brazil 1 Laboratório de Imunofarmacologia, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal Do Rio de Janeiro , Rio de Janeiro , Br |
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Author_xml | – sequence: 1 givenname: Luan surname: Firmino-Cruz fullname: Firmino-Cruz, Luan organization: Laboratório Interdisciplinar de Pesquisas Médicas, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil – sequence: 2 givenname: Debora surname: Decote-Ricardo fullname: Decote-Ricardo, Debora organization: Instituto de Veterinária, Universidade Federal Rural Do Rio de Janeiro, Seropédica, Brazil – sequence: 3 givenname: Daniel Claudio de Oliveira surname: Gomes fullname: Gomes, Daniel Claudio de Oliveira organization: Núcleo de Doenças Infecciosas/Núcleo de Biotecnologia, Universidade Federal Do Espírito Santo, Vitoria, Brazil – sequence: 4 givenname: Alexandre surname: Morrot fullname: Morrot, Alexandre organization: Faculdade de Medicina, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, Brazil – sequence: 5 givenname: Celio Geraldo surname: Freire-de-Lima fullname: Freire-de-Lima, Celio Geraldo organization: Laboratório de Imunomodulação, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, Brazil – sequence: 6 givenname: Herbert Leonel surname: de Matos Guedes fullname: de Matos Guedes, Herbert Leonel organization: Núcleo Multidisciplinar de Pesquisa UFRJ-Xerém em Biologia (NUMPEX-BIO), UFRJ Campus Duque de Caxias Professor Geraldo Cidade, Universidade Federal Do Rio de Janeiro, Duque de Caxias, Brazil |
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Cites_doi | 10.1128/IAI.73.4.2101-2108.2005 10.1093/intimm/8.11.1675 10.1371/journal.pone.0011445 10.1006/expr.1996.0102 10.1111/pim.12324 10.1074/jbc.M605146200 10.1016/j.micinf.2005.06.033 10.4049/jimmunol.1700943 10.1016/j.micinf.2017.11.004 10.1016/j.celrep.2016.05.028 10.3389/fimmu.2014.00535 10.1645/16-145 10.1111/j.1600-065X.1989.tb00557.x 10.1017/S0031182015000943 10.1146/annurev.iy.13.040195.001055 10.4049/jimmunol.0901114 10.4049/jimmunol.170.7.3819 10.1038/35003208 10.1016/j.imlet.2007.09.013 10.1186/s13071-016-1413-9 10.1111/j.1749-6632.1992.tb24591.x 10.1371/journal.pone.0124888 10.4049/jimmunol.1102880 10.3389/fimmu.2012.00372 10.1073/pnas.88.16.7011 10.4049/jimmunol.164.7.3681 10.3389/fimmu.2017.00518 10.1093/intimm/6.8.1117 10.1002/eji.200939455 10.4049/jimmunol.1002484 10.1073/pnas.89.8.3320 10.4331/wjbc.v8.i2.151 10.3389/fmicb.2017.00978 10.3109/08830189209055575 10.1111/pim.12661 10.1046/j.1365-2249.1999.00953.x 10.1073/pnas.0511305103 10.1016/j.cellimm.2018.08.014 10.3389/fmicb.2018.03056 10.1128/IAI.70.12.6597-6605.2002 10.1016/j.bbrc.2018.10.055 10.1016/0092-8674(93)90667-F 10.1016/j.ijpara.2007.08.010 |
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Copyright | Copyright © 2020 Firmino-Cruz, Decote-Ricardo, Gomes, Morrot, Freire-de-Lima and de Matos Guedes. Copyright © 2020 Firmino-Cruz, Decote-Ricardo, Gomes, Morrot, Freire-de-Lima and de Matos Guedes. 2020 Firmino-Cruz, Decote-Ricardo, Gomes, Morrot, Freire-de-Lima and de Matos Guedes |
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Keywords | BALB/XID Leishmaniasis B-1CDP cells IL-10 B-1 cells |
Language | English |
License | Copyright © 2020 Firmino-Cruz, Decote-Ricardo, Gomes, Morrot, Freire-de-Lima and de Matos Guedes. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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Title | How to B(e)-1 Important Cell During Leishmania Infection |
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