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. Author manuscript; available in PMC: 2017 Oct 1.
Published in final edited form as: Semin Hematol. 2016 Jul 25;53(4):230–236. doi: 10.1053/j.seminhematol.2016.07.003

Table 1.

The importance of allele and antigen mismatches on outcome after HLA-mismatched unrelated donor hematopoietic cell transplantation from marrow and peripheral blood stem cell graft sources.611 Low, intermediate and high risk refer to the relative risks associated with mismatching at the locus of interest.

Locus Marrow
Transplant
PBSC Transplant Risks Associated with Allele versus Antigen Mismatch
HLA-A High risk6 Intermediate
risk7
BM and PBSC: In general, allele mismatches are as risky
as antigen mismatches6,7
HLA-B Intermediate
risk6,7
Intermediate
risk6,7
BM: In general, allele mismatches are as risky as
antigen mismatches6
PBSC: limited numbers7
HLA-C Intermediate
risk6,7


High risk8
High risk6,7 In general, allele mismatches have lower risks than
antigen mismatches6,7,8
HLA-
DRB1
High risk6 The limited numbers prevent definitive analysis of
allele versus antigen.
HLA-
DQB1
Low risk6,7 Low risk6,7 Isolated mismatching at HLA-DQB1 is not associated
with higher risks.
HLA-
DPB1
High risk911 High risk911 The allele and antigen definitions are not applicable to
HLA-DP typing and nomenclature.2

BM, bone marrow

PBSC, peripheral blood stem cells