All T15 Id-positive antibodies (but not the majority of VHT15+ antibodies) are produced by peritoneal CD5+ B lymphocytes
- PMID: 1707658
- DOI: 10.1093/intimm/2.6.515
All T15 Id-positive antibodies (but not the majority of VHT15+ antibodies) are produced by peritoneal CD5+ B lymphocytes
Abstract
After adult irradiation and reconstitution with autologous bone marrow, BALB/c and C.B20 mice no longer utilize the T15 Id in response to phosphorylcholine. T15 Id expression can be restored by transfers of peritoneal B cells or by FACS-purified CD5+ IgM+ lymphocytes (but not by T lymphocytes) from syngeneic donors. Using bone marrow and peritoneal cell donors that are congeneic for heavy and light chain allotypes, the exclusive origin of the T15 Id in peritoneal B cells was ascertained. These conclusions have been essentially confirmed by immunization with either anti-T15 Id or anti-VHT15 antibodies conjugated to lipopolysaccharide. Thus, the production of VHT15-positive antibodies continues at control levels in bone marrow-reconstituted animals while no T15 Id production can be stimulated even in this protocol of direct B cell stimulation. These results constitute the first formal demonstration of the exclusive production of and Id by CD5+ B-cells.
Similar articles
-
Differential L chain expression in the antibody responses to phosphorylcholine of adult bone marrow or peritoneum-derived B lymphocytes.J Immunol. 1989 Jan 1;142(1):8-11. J Immunol. 1989. PMID: 2491875
-
Alterations of idiotypic profiles: the cellular basis of T15 dominance in BALB/c mice.J Mol Cell Immunol. 1987;3(5):307-20. J Mol Cell Immunol. 1987. PMID: 3509929
-
Origin of CD5+ B cells and natural IgM-secreting cells: reconstitution potential of adult bone marrow, spleen and peritoneal cells.Eur J Immunol. 1992 May;22(5):1243-51. doi: 10.1002/eji.1830220520. Eur J Immunol. 1992. PMID: 1374338
-
Coelomic and bone marrow-derived B cells. Developmental constraints versus antigen-specific selection.Ann N Y Acad Sci. 1992 May 4;651:433-42. doi: 10.1111/j.1749-6632.1992.tb24643.x. Ann N Y Acad Sci. 1992. PMID: 1376059 Review. No abstract available.
-
Cellular competition and the promotion of T15 to idiotypic dominance.Immunol Rev. 1989 Aug;110:119-34. doi: 10.1111/j.1600-065x.1989.tb00030.x. Immunol Rev. 1989. PMID: 2676845 Review. No abstract available.
Cited by
-
Host-derived lipids orchestrate pulmonary γδ T cell response to provide early protection against influenza virus infection.Nat Commun. 2021 Mar 26;12(1):1914. doi: 10.1038/s41467-021-22242-9. Nat Commun. 2021. PMID: 33772013 Free PMC article.
-
Long-term Immunotoxic Effects of Oral Prenatal and Neonatal Atrazine Exposure.Toxicol Sci. 2019 Apr 1;168(2):497-507. doi: 10.1093/toxsci/kfz005. Toxicol Sci. 2019. PMID: 30629250 Free PMC article.
-
ARID3a from the ARID family: structure, role in autoimmune diseases and drug discovery.Acta Pharmacol Sin. 2023 Nov;44(11):2139-2150. doi: 10.1038/s41401-023-01134-2. Epub 2023 Jul 24. Acta Pharmacol Sin. 2023. PMID: 37488425 Free PMC article. Review.
-
Facultative role of germinal centers and T cells in the somatic diversification of IgVH genes.J Exp Med. 1995 Apr 1;181(4):1319-31. doi: 10.1084/jem.181.4.1319. J Exp Med. 1995. PMID: 7535332 Free PMC article.
-
Content and dynamics of the human antibody variable region repertoire to the Haemophilus influenzae type b polysaccharide.Springer Semin Immunopathol. 1993;15(2-3):119-37. doi: 10.1007/BF00201096. Springer Semin Immunopathol. 1993. PMID: 8256194 Review. No abstract available.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources