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PMID: 6185616 Published · ppublish English Journal Article

Immune response to a thymus-dependent form of B512 dextran requires the presence of Lyb-5+ lymphocytes.

The Journal of experimental medicine ·Vol. 157 ·No. 2 ·1983-02-01 ·Pages 657-66

Stein KE, Zopf DA, Miller CB, Johnson BM, Mongini PK, Ahmed A, Paul WE

Abstract

Studies of the ontogeny of the immune response to B512 dextran (Dex) show that antibody responses equal to those of adult mice are not attained until 12 wk of age. We have examined the anti-Dex response after immunization with a thymus-dependent antigen isomaltohexaosyl-keyhole limpet hemocyanin (IM6-KLH) and have shown that the development of the cross-reacting anti-Dex response parallels the development of Lyb-5+ B cells. Adult levels of anti-Dex antibody after immunization with IM6-KLH are achieved in mice between 3 and 12 wk of age, a time when Lyb-5+ cells have reached adult levels. Neonatal mice, immunized at 1 d or 1 wk after birth, failed to produce a significant amount of anti-Dex antibodies, although they did produce IM6-specific antibodies after immunization with IM6-KLH. Data, which support the conclusion from these experiments that Lyb-5+ cells are required for an anti-polysaccharide response even when the immunizing antigen is thymus-dependent, include the failure of IM6-KLH to stimulate a normal anti-Dex response in mice with the xid defect and the direct demonstration in normal adult mice that elimination of Lyb-5+ cells from spleens of mice primed with IM6-KLH abolishes the ability of these cells to transfer an anti-Dex response. The data imply that the expressed B cell repertoire in adult animals is skewed such that the vast majority of B cells capable of responding to polysaccharide determinants are in the Lyb-5+ subset.

MeSH Terms
Animals Antigens, Ly/immunology B-Lymphocytes/immunology Dextrans/immunology Female Hemocyanins/immunology Immunoglobulin G/biosynthesis Immunoglobulin M/biosynthesis Isoantibodies/immunology Male Mice Mice, Inbred C57BL Mice, Inbred CBA Mice, Inbred DBA Oligosaccharides/immunology
Chemicals
Antigens, Ly Dextrans Immunoglobulin G Immunoglobulin M Isoantibodies Lyt antibodies Oligosaccharides isomaltohexose Hemocyanins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Stein K E
Zopf D A
Miller C B
Johnson B M
Mongini P K
Ahmed A
Paul W E
References (19)
19 references, click to expand
  1. X-linked genetic control of hapten-polysaccharide-mediated specific immune unresponsiveness in CBA/N mice.
    J Immunol. 1978 Apr;120(4):1362-8 PMID: 347000
  2. Inability of mice with a defect in B-lymphocyte maturation to respond to phosphorycholine on immunogenic carriers.
    J Exp Med. 1977 Oct 1;146(4):1138-42 PMID: 302313
  3. Induction of B cell priming by neonatal injection of mice with thymic-independent (type 2) antigens.
    J Immunol. 1978 Oct;121(4):1453-9 PMID: 359707
  4. Demonstration of phosphorylcholine-specific IgE B cells in CBA/N mice.
    J Immunol. 1979 Sep;123(3):1039-43 PMID: 381515
  5. Characteristics of the T-dependent alpha(1 leads to 6) glucosyl (dextran) antibody response induced in mice with isomaltohexaose coupled to chicken gamma-globulin.
    Eur J Immunol. 1979 Nov;9(11):916-9 PMID: 93549
  6. Antibody affinity in mice with the CBA/N defect.
    J Immunol. 1980 Apr;124(4):1798-802 PMID: 6767773
  7. Role of T lymphocytes in the response to TNP-AECM-Ficoll.
    J Immunol. 1980 Sep;125(3):1066-70 PMID: 6774013
  8. Role of accessory cells in B cell activation. II. The interaction of B cells with accessory cells results in the exclusive activation of an Lyb5+ B cell subpopulation.
    J Immunol. 1980 Sep;125(3):1340-8 PMID: 6157725
  9. CBA/N X BALB/cJ F1 male and female mice can be primed to express quantitatively equivalent secondary anti-phosphocholine responses.
    J Immunol. 1981 Jan;126(1):387-9 PMID: 7451980
  10. Antitrinitrophenyl (TNP) plaque assay. Primary response of Balb/c mice to soluble and particulate immunogen.
    Proc Soc Exp Biol Med. 1969 Nov;132(2):575-81 PMID: 5355110
  11. Lack of neonatal susceptibility to induction of tolerance by polysaccharide antigens.
    Eur J Immunol. 1976 Jul;6(7):486-92 PMID: 1086789
  12. Identification of a B-cell surface structure involved in antigen-dependent triggering: absence of this structure on B cells from CBA/N mutant mice.
    J Exp Med. 1977 Jan 1;145(1):10-20 PMID: 299766
  13. B-lymphocyte heterogeneity: development and characterization of an alloantiserum which distinguishes B-lymphocyte differentiation alloantigens.
    J Exp Med. 1977 Jan 1;145(1):101-10 PMID: 299767
  14. T-independent responses in B cell-defective CBA/N mice to Brucella abortus and to trinitrophenyl (TNP) conjugates of Brucella abortus.
    Eur J Immunol. 1978 Jul;8(7):459-63 PMID: 99320
  15. Surface immunoglobulin D as a functional receptor for a subclass of B lymphocytes.
    Immunol Rev. 1977;37:89-104 PMID: 338469
  16. Immune response to phosphorylcholine. VIII. The response CBA/N mice to PC-LPS.
    J Immunol. 1981 May;126(5):1790-3 PMID: 7217666
  17. Altered idiotype response to phosphocholine in mice bearing an x-linked immune defect.
    J Immunol. 1981 Oct;127(4):1629-33 PMID: 7196930
  18. The immune response to an isomaltohexosyl-protein conjugate, a thymus-dependent analogue of alpha(1 replaced by 6) dextran.
    J Immunol. 1982 Mar;128(3):1350-4 PMID: 6173433
  19. Carbohydrate antigens: coupling of oligosaccharide phenethylamine-isothiocyanate derivatives to bovine serum albumin.
    Methods Enzymol. 1978;50:169-71 PMID: 661573
Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1983-02-01
Pages
657-66
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2186926
Subset
IM
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