Minor histocompatibility antigens on canine hemopoietic progenitor cells

Martin Weber, Claudia Lange, Wolfgang Günther, Monika Franz, Elisabeth Kremmer, Hans Jochem Kolb

Research output: Contribution to journalArticlepeer-review

23 Scopus citations


Adoptive immunotherapy with CTL against minor histocompatibility Ags (mHA) provides a promising way to treat leukemia relapse in allogeneic chimeras. Here we describe the in vitro generation of CTL against mHA in the dog. We tested their inhibitory effect on the growth of hemopoietic progenitor cells stimulated by hemopoietic growth factors in a 4-day suspension culture. CTL were produced by coculture of donor PBMC with bone marrow-derived dendritic cells (DCs). These DCs were characterized by morphology, high expression of MHC class II and CD1a, and the absence of the monocyte-specific marker CD14. Characteristically these cells stimulated allogeneic lymphocytes (MLR) and, after pulsing with a foreign Ag (keyhole limpet hemocyanin), autologous T cells. CTL were generated either ex vivo by coculture with DCs of DLA-identical littermates or in vivo by immunization of the responder with DCs obtained from a DLA-identical littermate. In suspension culture assays the growth of hemopoietic progenitor cells was inhibited in 53% of DLA-identical littermate combinations. In canine families mHA segregated with DLA as restriction elements. One-way reactivity against mHA was found in five littermate combinations. In two cases mHA might be Y chromosome associated, in three cases autosomally inherited alleles were detected. We conclude that CTL can be produced in vitro and in vivo against mHA on canine hemopoietic progenitor cells using bone marrow-derived DCs.

Original languageEnglish
Pages (from-to)5861-5868
Number of pages8
JournalJournal of Immunology
Issue number12
StatePublished - 15 Jun 2003
Externally publishedYes


Dive into the research topics of 'Minor histocompatibility antigens on canine hemopoietic progenitor cells'. Together they form a unique fingerprint.

Cite this