Literature DB >> 9361968

Alloresponses to HLA-DP detected in the primary MLR: correlation with a single amino acid difference.

I Nicholson1, M Varney, C Kanaan, A Grigg, J Szer, K Tiedemann, B D Tait.   

Abstract

The one-way mixed lymphocyte reaction (MLR-1) response was measured in both directions in 50 HLA-A, B, DR and DQ identical pairs and the role of DP studied in MLR stimulation. DR, DQ and DP typing was performed at the allele level by the polymerase chain reaction-sequence specific oligotyping (PCR-SSO) technique. The group consisted of 19 potential bone marrow transplant recipients and 34 matched unrelated donors. When more than one matched donor was available for a patient, donor/donor MLR-1 was also studied. DP identity was observed in 3 out of 50 pairs (6%), however due to homozygosity no incompatibility was present in the stimulating cells in 21 out of 100 cases (21%). There was a significant difference in the range of relative responses (RR) between zero DPB1 mismatches and one (p = 0.002) and two (p = 0.02) DPB1 mismatches: 52.4% of cases in the zero DPB1 mismatch group had RR < 1.0% compared with 31.6% and 27.3% in the one and two DPB1 mismatches. Stimulation by DPB1*0201 and 0301 gave the highest RR (12.9 +/- 22.5 and 17.5 +/- 17.0, respectively) while stimulation with DPB1*0401 and 0402 resulted in low levels of T cell response (1.3 +/- 8.2 and 0.6 +/- 11.5, respectively). When the responses were restricted to DPB1*0401 homozygotes to standardise for responder type similar results were obtained (DPB1*0201 v DPB1*0402 p = 0.008). The protein products of the DPB1*0201 and 0402 alleles differ by a single amino acid at position 69 (DPB1*0402--Lysine, DPB1*0201--glutamic acid). A further analysis was performed therefore scoring responders and stimulators as glutamic acid positive (E+) or negative (E-). There was a highly significant increase in the response to E+ stimulators compared with E- stimulators (p = 0.004). There was also a significant difference in the distribution of relative responses between the E+ stimulator group and the subgroups of E- responders/E- stimulators (p = 0.012) and E+ responders/E- stimulators (p = 0.009). However the amino acid difference at position 69 does not explain all responses due to DP in the MLR-1 as evidenced by the strong responses observed in cases where DPB1*0301 (lysine pos.) was the only difference on the stimulator cells. The results indicate that not all DP incompatibilities elicit a measurable T cell MLR response, but where a response does occur residue 69 in the first domain of DP appears to be pivotal. These results may have implications with respect to GVHD in bone marrow transplantation.

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Year:  1997        PMID: 9361968     DOI: 10.1016/s0198-8859(97)00091-8

Source DB:  PubMed          Journal:  Hum Immunol        ISSN: 0198-8859            Impact factor:   2.850


  9 in total

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Journal:  Lancet Oncol       Date:  2012-02-15       Impact factor: 41.316

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Authors:  Janelle A Noble; Ana M Valdes
Journal:  Curr Diab Rep       Date:  2011-12       Impact factor: 4.810

3.  HLA DPA1, DPB1 alleles and haplotypes contribute to the risk associated with type 1 diabetes: analysis of the type 1 diabetes genetics consortium families.

Authors:  Michael D Varney; Ana Maria Valdes; Joyce A Carlson; Janelle A Noble; Brian D Tait; Persia Bonella; Eva Lavant; Anna Lisa Fear; Anthony Louey; Priscilla Moonsamy; Josyf C Mychaleckyj; Henry Erlich
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Journal:  PLoS One       Date:  2011-03-08       Impact factor: 3.240

5.  ATPase4A Autoreactivity and Its Association With Autoimmune Phenotypes in the Type 1 Diabetes Genetics Consortium Study.

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6.  Alloreactive T Cell Receptor Diversity against Structurally Similar or Dissimilar HLA-DP Antigens Assessed by Deep Sequencing.

Authors:  Esteban Arrieta-Bolaños; Pietro Crivello; Maximilian Metzing; Thuja Meurer; Müberra Ahci; Julie Rytlewski; Marissa Vignali; Erik Yusko; Peter van Balen; Peter A Horn; J H Frederik Falkenburg; Katharina Fleischhauer
Journal:  Front Immunol       Date:  2018-02-19       Impact factor: 7.561

7.  The allogeneic HLA-DP-restricted T-cell repertoire provoked by allogeneic dendritic cells contains T cells that show restricted recognition of hematopoietic cells including primary malignant cells.

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Journal:  Haematologica       Date:  2018-09-20       Impact factor: 9.941

8.  Promiscuity of Peptides Presented in HLA-DP Molecules from Different Immunogenicity Groups Is Associated With T-Cell Cross-Reactivity.

Authors:  Aicha Laghmouchi; Michel G D Kester; Conny Hoogstraten; Lois Hageman; Wendy de Klerk; Wesley Huisman; Eva A S Koster; Arnoud H de Ru; Peter van Balen; Sebastian Klobuch; Peter A van Veelen; J H Frederik Falkenburg; Inge Jedema
Journal:  Front Immunol       Date:  2022-02-16       Impact factor: 7.561

9.  Genetic variants in human leukocyte antigen-DP influence both hepatitis C virus persistence and hepatitis C virus F protein generation in the Chinese Han population.

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Journal:  Int J Mol Sci       Date:  2014-06-03       Impact factor: 5.923

  9 in total

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