Literature DB >> 14013738

Acquired tolerance to skin homografts in mice. I. Histological analysis of lymphoid tissues before, during, and after the loss of tolerance.

B F ARGYRIS.   

Abstract

Acquired tolerance to CBA skin homografts is lost in a large number of C3H mice neonatally injected with CBA spleen cells. The skin homografts persist for at least 2 months but then exhibit a chronic rejection pattern which may last up to 7 months. Histological analysis of the lymphoid tissues reveals the onset of an immune response in the axillary lymph nodes of many 4-month-old tolerant mice. This immune response which appears before external indications of graft rejection are evident, is manifested as an increase in number of germinal centers and plasma cells in the cortex and medulla, respectively. In older tolerant mice, an even larger proportion show these histological indications of immunological activity. During graft contraction and shortly after graft rejection, the immune response is still limited to the lymph nodes. After rejection of a second graft by post-tolerant mice, histological indications of an immune response are not only found in lymph nodes but also in spleen. The data suggest the development of a host versus graft reaction in seemingly tolerant C3H mice, which increases in severity with the age of the animal. The results are discussed from the point of view that tolerance is dependent upon a critical balance between the immune potential of the host and the population of donor cells. As mice mature, their immune potential may increase. The resulting host versus graft reaction increases, culminating in the rejection of skin graft and donor lymphoid cells.

Entities:  

Keywords:  LYMPHOID TISSUE; SKIN TRANSPLANTATION

Mesh:

Year:  1963        PMID: 14013738      PMCID: PMC2180443          DOI: 10.1084/jem.117.3.543

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  14 in total

1.  Elimination of runt disease and induction of acquired tolerance by x-irradiated spleen cells.

Authors:  B F ARGYRIS
Journal:  Plast Reconstr Surg       Date:  1962-01       Impact factor: 4.730

2.  Quantitative studies on the induction of tolerance of skin homografts and on runt disease in neonatal rats.

Authors:  R E BILLINGHAM; W K SILVERS; D STEINMULLER
Journal:  J Natl Cancer Inst       Date:  1962-02       Impact factor: 13.506

3.  Abolition of neonatally-induced homograft tolerance in mice by sublethal x-irradiation.

Authors:  A FEFER; G J NOSSAL
Journal:  Plast Reconstr Surg       Date:  1962-04       Impact factor: 4.730

4.  Radiation chimeras.

Authors:  P C KOLLER; A J DAVIES; S M DOAK
Journal:  Adv Cancer Res       Date:  1961       Impact factor: 6.242

5.  Studies on homologous disease. I. Factors concerned in the production of homologous disease of mice.

Authors:  J W JUTILA; R S WEISER
Journal:  J Immunol       Date:  1962-05       Impact factor: 5.422

6.  The runting syndrome.

Authors:  G SISKIND; L LEONARD; L THOMAS
Journal:  Ann N Y Acad Sci       Date:  1960-05-31       Impact factor: 5.691

7.  Cellular changes in lymph nodes and spleen following skin homografting in the rabbit.

Authors:  R J SCOTHORNE; I A MCGREGOR
Journal:  J Anat       Date:  1955-07       Impact factor: 2.610

8.  Relative antibody-forming capacity of spleen cells as a function of age.

Authors:  T MAKINODAN; W J PETERSON
Journal:  Proc Natl Acad Sci U S A       Date:  1962-02       Impact factor: 11.205

9.  Sequence of cellular responses to injury in mice exposed to 1,000 r total-body x-radiation.

Authors:  J BARROW; J L TULLIS
Journal:  AMA Arch Pathol       Date:  1952-05

10.  Effects of internal irradiation of mice with P32. I. Spleen, lymph nodes, thymus, bone and bone marrow.

Authors:  S WARREN; J C MacMILLAN; F J DIXON
Journal:  Radiology       Date:  1950-09       Impact factor: 11.105

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