B-1 cell origins and V(H) repertoire determination

Current Topics in Microbiology and Immunology

Volumn 252, Issue , 2000, Pages 3-13

  Herzenberg, L A ^a   Baumgarth, N ^a   Wilshire, J A ^a  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

IMMUNOGLOBULIN HEAVY CHAIN;

B LYMPHOCYTE; CONFERENCE PAPER; HUMAN; IMMUNOGLOBULIN GENE; IMMUNOGLOBULIN VARIABLE REGION; MULTIGENE FAMILY; NONHUMAN; PRIORITY JOURNAL; STEM CELL;

EID: 0033762333     PISSN: 0070217X     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-3-642-57284-5_1     Document Type: Conference Paper

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4. B-cell lineages exist in the mouse
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7. Surface markers, heavy chain sequences and B cell lineages
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9. CD5+ B-cell networks
10. B cell development in mice
11. An embryonic source of Ly1 but not conventional B cells
12. The fetal omentum in mice and humans. A site enriched for precursors of CD5 B cells early in development
13. The human fetal omentum: A site of B cell generation
14. Para-aortic splanchnopleura from early mouse embryos contains B 1 a cell progenitors
15. Antigenic phenotype and gene expression pattern of lymphohemopoietic progenitors during early mouse ontogeny
16. Isolation of peritoneal precursors of B-1 cells in the adult mouse
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19. Feedback regulation of murine Ly-1 B cell development
20. A novel regulatory myosin light chain gene distinguishes pre-B cell subsets and is IL-7 inducible
21. Absence of MHC class II expression distinguishes fetal from adult B lymphopoiesis in mice
22. Major histocompatibility complex class II expression distinguishes two distinct B cell developmental pathways during ontogeny
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24. A novel mechanism for B cell repertoire maturation based on response by B cell precursors to pre-B receptor assembly
25. Differential development of progenitor activity for three B cell lineages
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27. An unbiased analysis of V(H)-DJ(H) sequences from B-1a, B-1b, and conventional B cells
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29. Interleukin 9-induced in vivo expansion of the B-1 lymphocyte population
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31. The peritoneal Ly-1 (CD5) B cell repertoire is unique among murine B cell repertoires
32. Autoantibodies to phosphatidylcholine. The murine antibromelain RBC response
33. Phosphatidyl choline is recognized by a series of Ly-1+ murine B cell lymphomas specific for erythrocyte membranes
34. Self-tolerance maintained by active suppressor mechanisms
35. All VH11 genes expressed in peritoneal lymphocytes encode anti-bromelain-treated mouse red blood cell autoantibodies but othe rVH gene families contribute to this specificity
36. Studies of the antigenicity and immunogenicity of bromelain-pretreated red blood cells
37. Precommitment of normal mouse peritoneal cells by erythrocyte antigens in relation to auto-antibody production
38. A critical role of natural immunoglobulin M in immediate defense against systemic bacterial infection
39. Prominent V(H) genes expressed in innate antibodies are associated with distinctive antigen-bindings sites (J(H)-CDR3)
40. Development of B-1 Cells: Segregation of phosphatidyl choline-specific B cells to the B-1 population occurs after immunoglobulin gene expression
41. Mechanisms that limit the diversity of antibody: Three sequentially acting mechanisms that favor the spontaneous production of germ-line encoded anti-phosphatidyl choline
42. Mechanisms that limit the diversity of antibodies. II. Evolutionary conservation of Ig variable region genes which encode naturally occurring autoantibodies
43. The CH series of murine B cell lymphomas: Neoplastic analogues of Ly-1+ normal B cells
44. Normal mouse peritoneum contains a large population of Ly-1+ (CD5) B cells that recognize phosphatidyl choline. Relationship to cells that secrete hemolytic antibody specific for autologous erythrocytes
45. The I binding specificity of human VH 4-34 (VH 4-21) encoded antibodies is determined by both VH framework region 1 and complementarity determining region 3
46. Staphylococcal protein A binding to VH3 encoded immunoglobulins
47. The majority of murine VH12-expressing B cells are excluded from the peripheral repertoire in adults