4.3 Article

Differential HLA class I subunit (A, B, C heavy chain and β2-microglobulin) expression levels in normal tissues

Journal

VIRCHOWS ARCHIV
Volume 482, Issue 2, Pages 359-368

Publisher

SPRINGER
DOI: 10.1007/s00428-022-03459-5

Keywords

HLA class I; HLA-ABC; beta 2-microglobulin; TMA; Healthy tissues

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The expression level of HLA class I subunits in primary and metastatic lesions has been studied in various cancer types. However, there is limited information about HLA class I subunit expression in normal tissues. In this study, the expression level of HLA-A, HLA-B, HLA-C heavy chains, and beta 2-microglobulin was examined in normal tissues. The results showed that HLA class I subunit expression is not detectable in all nucleated cells, but is found only at the endothelial level. This information is important for evaluating changes in HLA class I subunit expression associated with malignant cell transformation.
Human leukocyte antigen (HLA) class I subunit expression level in primary and metastatic lesions has been characterized in many cancer types utilizing formalin-fixed and paraffin-embedded (FFPE) tissue sections as substrates in immunohistochemical reactions. The evaluation of the results of these studies has been hampered by the scant information about HLA class I subunit expression level in normal tissues. To address this unmet need, we have analyzed the HLA class I subunit expression level in FFPE sections of normal tissues. Two tissue microarray (TMA) blocks were constructed from archived FFPE tissue samples of a wide number of human normal tissues. The expression level of HLA-A, HLA-B, HLA-C heavy chains and beta 2-microglobulin (beta 2-M) was evaluated by IHC staining, with mAb HC-A2, mAb HC-10, and mAb NAMB1, respectively. The staining was scored according to its intensity. According to their staining patterns with the three mAbs tested, normal tissues can be divided into four groups: (i) tissues displaying moderate/strong staining patterns, (ii) tissues displaying barely detectable staining patterns, (iii) tissues displaying differential staining patterns, and (iv) tissues with no detectable staining. The ubiquitous expression pattern for HLA-A, B, C heavy chain and beta 2-M was found only at the endothelial level; the stroma was negative except for fibroblasts in all the tissues analyzed. Our data suggest that, contrary to the general postulate, HLA class I subunit expression is not detectable in all nucleated cells. This information provides a useful background to evaluate changes in HLA class I subunit expression associated with the malignant transformation of cells.

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