CD5 is a potential selecting ligand for B cells surface immunoglobulin framework region sequences

Journal of Experimental Medicine

Volumn 184, Issue 4, 1996, Pages 1279-1284

  Pospisil, Richard ^a,b   Fitts, Matthew G ^a   Mage, Rose G ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b INSTITUTE OF MICROBIOLOGY   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

CD5 ANTIGEN; GLYCOPROTEIN;

ANIMAL CELL; ANTIGEN ANTIBODY COMPLEX; ARTICLE; AUTOIMMUNITY; CELL MATURATION; CELL SURFACE; CELL TRANSFORMATION; GENE EXPRESSION; HAPLOTYPE; IMMUNOGLOBULIN BLOOD LEVEL; LIGAND BINDING; NONHUMAN; ONTOGENY; PRIORITY JOURNAL; RABBIT;

ANIMALS; ANTIGENS, CD5; APPENDIX; B-LYMPHOCYTES; CHROMATOGRAPHY, AFFINITY; GENE REARRANGEMENT, B-LYMPHOCYTE, HEAVY CHAIN; IMMUNOGLOBULIN FAB FRAGMENTS; IMMUNOGLOBULIN HEAVY CHAINS; IMMUNOGLOBULIN VARIABLE REGION; LYMPHOCYTE ACTIVATION; RABBITS;

EID: 0029946406     PISSN: 00221007     EISSN: None     Source Type: Journal    
DOI: 10.1084/jem.184.4.1279     Document Type: Article

References (34)

1. Nemazee, P.A., and K. Burki. 1989. Clonal deletion of autoreactive B lymphocytes in bone marrow chimeras. Proc. Natl. Acad. Sci. USA. 86:8039-8043.
2. Nemazee, P.A., and K. Burki. 1989. Clonal deletion of B lymphocytes in a transgenic mouse bearing anti-MHC class I antibody genes. Nature (Lond.). 337:562-566.
3. Tiegs, S.L., D.M. Russell, and D. Nemazee. 1993. Receptor editing in self-reactive bone marrow B cells. J. Exp. Med. 177:1009-1020.
4. Gay, D., T. Saunders, S. Camper, and M. Weigert. 1993. Receptor editing: an approach by autoreactive B cells to escape tolerance. J. Exp. Med. 177:999-1008.
5. Nossal, G.J.V. 1983. Cellular mechanisms of immunological tolerance. Annu. Rev. Immunol. 1:33-62.
6. Goodnow, C.C. 1992. Transgenic mice and analysis of B-cell tolerance. Annu. Rev. Immunol. 10:489-518.
7. Schwartz, R.H. 1989. Acquisition of immunologic tolerance. Cell. 57:1073-1081.
8. Pandey, A., L.W. Tjoelker, and C.B. Thompson. 1993. Restricted immunoglobulin junctional diversity in neonatal B cells results from developmental selection rather than homology-based V(D)J joining. J. Exp. Med. 177:329-337.
9. H gene family expression in immunoglobulin-transgenic mice: evidence for selection of antibody repertoires. Int. Immunol. 3:67-73.
10. Schwartz, R.S., and B.D. Stollar. 1994. Heavy-chain directed B-cell maturation: continuous clonal selection beginning at the pre-B cell stage. Immunol. Today. 15:27-32.
11. Silverman, G.J. 1994. Superantigens and the spectrum of unconventional B-cell antigens. Immunologist. 2:51-57.
12. Zouali, M. 1995. B-cell superantigens: implications for selection of the human antibody repertoire. Immunol. Today. 16: 399-405.
13. H allotypes, implications for the generation of antibody diversity. Cell. 60: 963-970.
14. H genes in leukemic rabbit B cells. Eur. J. Immunol. 20:397-402.
15. Ha allotype gene that is deleted in Alicia mutants; somatic hypermutation/conversion may play a major role in generating the heterogeneity of rabbit heavy chain variable region sequences. Eur. J. Immunol. 21:411-417.
16. Ha allotypes of the rabbit. Mol. Immunol. 21:1067-1081.
17. Kelus, A.S., and S. Weiss. 1986. Mutation affecting the expression of immunoglobulin variable regions in the rabbit. Proc. Natl. Acad. Sci. USA. 83:4883-4886.
18. H-mutant rabbits. Proc. Natl. Acad. Sci. USA 92:6961-6965.
19. + B cells predominate in peripheral tissues of rabbit. J. Immunol. 149:3858-3864.
20. Abdi, B.H., L.R. Wilder, I. Scher, and R.G. Mage. 1980. Surface immunoglobulin of rabbit peripheral blood lymphocytes: detection of allotypes by fluorescence and rosetting. Eur. J. Immunol. 10:852-859.
21. H antiserum. Mol. Immunol. 17:71-80.
22. Reinherz, E.L., P.C. Kung, G. Goldstein, and S.F. Schlossman. 1979. A monoclonal antibody with selective reactivity with functionally mature human thymocytes and all peripheral human T cells. J. Immunol. 123:1312-1317.
23. Fiebig, H., I. Behn, U. Hommel, H. Kupper, and W. Eichler. 1989. In Leucocyte Typing IV. W. Knapp et al., editors. Oxford University Press. Oxford. 332-335.
24. H sequences by gene conversion. Comments on a theory of the ontogeny of the chicken humoral immune system: the consequences of diversification by gene hyperconversion and its extension ro rabbit. Res. Immunol. 144:476-183.
25. Lankester, A.C., G.M.V. van Schijndel, J.L. Cordell, C.J.M. van Noesel, and R.A.W. van Lier. 1994. CD5 is associated with the human B cell antigen receptor complex. Eur. J. Immunol. 24:812-816.
26. Kozlowski, L.M., S.R. Kunning, Y. Zheng, L.M. Wheatley, and A.I. Levinson. 1995. Staphylococcus aureus Cowan I-induced human immunoglobulin responses: preferential IgM rheumatoid factor production and VH3 mRNA expression by protein A-binding B cells. J. Clin. Immunol. 15:145-151.
27. Kipps, T.J. 1989. The CD5 B cell. Adv. Immunol. 47:117-185.
28. + B lymphocytes, polyreactive antibodies and the human B-cell repertoire. Immunol. Today. 10:364-368.
29. + B cells. Immunol. Rev. 137:91-118.
30. Tarkhovsky, A., S.B. Kanner, J. Hombach, J.A. Ledbetter, W. Muller, N. Killeen, and K. Rajewsky. Science (Wash. DC). 269:535-537.
31. Boumsell, L., A. Bernard, V. Lepage, L. Degos, J. Lemerle, and J. Dausset. 1978. Some chronic lymphocytic leukemia cells bearing surface immunoglobulines share determinants with T cells. Eur. J. Immunol. 8:900-904.
32. Van de Velde, H., I. von Hoegen, W. Luo, J.R. Parnes, and K. Thielemans. 1991. The B-cell surface protein CD72/Lyb-2 is the ligand for CD5. Nature (Lond.). 351:662-665.
33. Chen, X., Y. Matsuura, and J.F. Kearney. 1995. CD5 transfenic mice. Curr. Top. Microbiol. Immunol. 95:209-217.
34. Cyster, J.G., J.I. Healy, K. Kishihara, T.W. Mak, M.L. Thomas, and C.C. Goodnow. 1996. Regulation of B-lymphocyte negative and positive selection by tyrosine phosphatase CD45. Nature (Lond.). 381:325-328.