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PMID: 4129803 Published · ppublish English Journal Article

Two separate genes controlling stimulation in mixed lymphocyte reaction in man.

Dupont B, Good RA, Hansen GS, Jersild C, Nielsen LS, Park BH, Svejgaard A, Thomsen M, Yunis EJ

Abstract

The genetic control of strong stimulation in the mixed lymphocyte culture reaction is determined by a separate gene (MLR-S) closely linked to the FOUR-locus of the HL-A chromosomal region. Three additional examples of siblings with recombination between FOUR-locus and MLR-S locus are presented which confirms the independent genetic control of mixed lymphocyte reaction from the control of HL-A antigens. The occurrence of two recombinant children in one family with four other children representing all possible HL-A haplotype-combinations, strongly supports the genetic mapping of the MLR-S determinants outside the HL-A chromosomal region. The experiments presented show that additional genes located within the HL-A region itself contribute with a weak stimulation of allogenic mixtures. These data are discussed in relation to the marginal stimulation of the mixed lymphocyte culture reaction which can be seen between unrelated individuals. It seems that a group of relatively histocompatible individuals can be defined by identity of the MLR-S locus but with differences on the weak MLC-determinants, and that this group for the purpose of clinical transplantation behaves as histocompatible individuals.

MeSH Terms
Adult Child Chromosome Mapping Epitopes Female Genes Genetic Linkage Genotype Histocompatibility Antigens Humans Lymphocyte Activation Lymphocyte Culture Test, Mixed Male Mitomycins Models, Biological Pedigree Recombination, Genetic
Chemicals
Epitopes Histocompatibility Antigens Mitomycins
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Dupont B
Good R A
Hansen G S
Jersild C
Nielsen L S
Park B H
Svejgaard A
Thomsen M
Yunis E J
References (14)
14 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1974-01-00
Pages
52-6
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC387930
Subset
IM
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