Immune function in fully allogeneic mouse bone marrow chimeras

Susan E. Krown, Richard Coico, Margrit P. Scheid, Gabriel Fernandes, Robert A. Good

Research output: Contribution to journalArticle

48 Scopus citations

Abstract

Stable, long-lived, immunologically functional H-2 allogeneic chimeras, free of graft vs host disease, were established by reconstituting irradiated CBA J (H-2k) mice with C57BL 6 (H-2b) bone marrow, previously depleted of Thy 1+ cells with monoclonal anti-Thy 1.2 (mc-α-Thy 1.2) serum and complement (C). All lymph node cells of these chimeras expressed the donor H-2 phenotype, while a small, significant number of cells expressing host H-2 determinants were detectable in the spleens of the chimeras throughout the period of investigation. Skin graft rejection pattern, MLC, and CML responses of chimeric mice were normal against third-party targets, but reflected complete tolerance against donor and host determinants. NK activity against tumor cell targets was also normal. The host-like pattern of chimeric ADCC response against chicken red blood cells suggested the persistent activity of host macrophages. In contrast to the reduced primary PFC response against SRBC, the vigorous secondary response of the chimeras suggested that haplotype restrictions are not absolutely binding when there is an opportunity for prior learning.

Original languageEnglish (US)
Pages (from-to)268-283
Number of pages16
JournalClinical Immunology and Immunopathology
Volume19
Issue number2
DOIs
StatePublished - May 1981

ASJC Scopus subject areas

  • Immunology and Allergy
  • Pathology and Forensic Medicine
  • Immunology

Fingerprint Dive into the research topics of 'Immune function in fully allogeneic mouse bone marrow chimeras'. Together they form a unique fingerprint.

  • Cite this

    Krown, S. E., Coico, R., Scheid, M. P., Fernandes, G., & Good, R. A. (1981). Immune function in fully allogeneic mouse bone marrow chimeras. Clinical Immunology and Immunopathology, 19(2), 268-283. https://doi.org/10.1016/0090-1229(81)90069-6