In a family with a maternal DR/GLO recombination, cellular DP typing s
howed it to be located between DR and DP. RFLB studies done during the
9th international histocompatibility workshop gave anomalous segregat
ion patterns of DPA and DPB bands that could be interpreted as being d
ue to a second, paternal DR/DP recombination. This assumption was conf
irmed later by PCR-SSO typing. A more precise mapping has been done by
new markers showing the maternal recombination to be within the TAP2
locus and the paternal recombination to be between DQB1 and DQB3. This
supports earlier suggestions of a hot spot of recombination in the TA
P region. The recombinations involve parental haplotypes that presentl
y show DR/DP linkage disequilibrium in the French population and it is
proposed that DR/DP recombinations occur randomly while B/DR recombin
ations preferentially occur on haplotypes without strong linkage diseq
uilibrium. Existing DR/DP linkage disequilibria in a given population
will thus be broken down with time. The mixed lymphocyte culture respo
nse towards an isolated DP difference was tested in this and another D
R/DP recombinant family. It showed that an alloresponse towards DP may
be highly variable and this suggests that it might be important to de
fine the rules for the strength of this reaction and the possible impl
ications for allotransplantation.