SERUM IMMUNOGLOBULIN ISOTYPE PROFILE OF VIABLE AND NON VIABLE LYMPHOID CELL CHIMAERAS MADE WITH NUDE ATHYMIC Ipr (LYMPHOPROLIFERATION) MOUSE RECIPIENTS
- 1 January 1992
- journal article
- research article
- Published by Taylor & Francis in Autoimmunity
- Vol. 11 (3) , 151-158
- https://doi.org/10.3109/08916939209035149
Abstract
C57BL/6 mice (B6) which are homozygous at the nu (nude, athymic) and Ipr (lymphoproliferation) locus (B6 nulpr) are short-lived. We showed previously that increased survival could be obtained by grafting lymphoid cells from euthymic /pr-homozygous B6 mice (B6 Ipr) mice ([Ipr → nulpr] chimaeras), but curiously enough not from normal (B6 wild) mice ([wild → nulpr] chimaeras). Moreover female, but not male, [Ipr→ tnulpr] chimaeras developed spleen and lymph node enlargement. In the present paper the distribution and absolute concentrations of all serum immunoglobulin (Ig) isotypes have been determined in these chimaeras and their controls. All chimaeras displayed whole serum Ig levels higher than those of B6 wild mice, suggesting a successful reconstitution of the athymic recipients by the grafted lymphoid cells, but two types of chimaeras were peculiar. The short-lived [wild → nulpr] chimaeras showed a proportion of IgM as high as ungrafted B6 nulpr mice, suggesting a deficient down-regulation of IgM production by the grafted B6 wild-type lymphoid cells. The [Ipr→ tnulpr] female chimaeras recovered a long lasting overexpression of all Ig isotypes, like B6 Ipr mice, while all the other chimaeras showed a transient overexpression only. Since neither lymphadeno-pathy nor persistent increase of serum Ig levels were observed in [Ipr → nu] chimaeras, our data confirmed the need for a genetically Ipr host to allow the significant development of the Ipr syndrome.Keywords
This publication has 16 references indexed in Scilit:
- Immunoglobulin isotypes of c57bl/6 nu/nu, lpr/ lpr mice. Lack of direct intrinsic effect of the lpr gene on b cell hyperactivityAutoimmunity, 1991
- Bone marrow transplantation from mutantlpr/lpr mice. Functional abnormalities rather than alloantigenic differences appear to determine the development of a graft-vs. -host-like syndromeEuropean Journal of Immunology, 1990
- Common and individual features of the humoral immunity dysregulation of mice homozygous at the viable motheaten (mev) mutationImmunology Letters, 1990
- Reciprocal Lymphoid Cell Homing Studies Using Wild and LPR (Lymphoproliferation) Mutant C57Bl MICEAutoimmunity, 1990
- Serum concentrations of IgM, IgG1, IgG2b, IgG3 and IgA in C57BL6 mice and their congenics at the lpr (lymphoproliferation) locusJournal of Autoimmunity, 1989
- Hyper-Ia antigen expression on B cells from - mice correlates with manifestations of the autoimmune stateClinical Immunology and Immunopathology, 1985
- Mechanisms of polyclonal B-cell activation in autoimmune B6-lpr/lpr miceCellular Immunology, 1984
- Identification of a B cell differentiation factor(s) spontaneously produced by proliferating T cells in murine lupus strains of the lpr/lpr genotype.The Journal of Experimental Medicine, 1983
- Thymic Influences on Autoimmunity in MRL‐1pr MiceScandinavian Journal of Immunology, 1982
- A y chromosome associated factor in strain bxsb producing accelerated autoimmunity and lymphoproliferationArthritis & Rheumatism, 1979