| Literature DB >> 34617807 |
Akiya Kogami1, Mana Fukushima1,2, Hitomi Hoshino1, Takuya Komeno3, Tadakazu Okoshi4, Masataka Murahashi1, Tomoya O Akama5, Junya Mitoma6, Haruo Ohtani7, Motohiro Kobayashi1,2.
Abstract
Angioimmunoblastic T-cell lymphoma (AITL) is a T-cell lymphoma of follicular helper T-cell origin. Histologically, neoplastic T-cells proliferate to form clusters adjacent to or between arborizing high endothelial venules (HEVs). HEVs in normal lymph nodes express sulfated glycans called peripheral lymph node addressin (PNAd); however, it remains unclear whether PNAd is also expressed on HEVs in AITL. Furthermore, although it is widely accepted that HEVs are conspicuous in AITL due to their proliferation, quantitative histological support for this concept is lacking. To investigate these issues, we employed monoclonal antibodies recognizing PNAd, namely, MECA-79, HECA-452, and 297-11A, and performed quantitative immunohistochemical analysis of HEVs in 36 AITL-affected and 67 normal lymph nodes. Staining with all three antibodies confirmed that AITL HEVs express PNAd. Moreover, AITL HEVs were bound calcium-dependently by L-selectin-IgM fusion proteins, indicating that they function in the recruitment of L-selectin-expressing lymphocytes. Unexpectedly, HEV distribution density was not increased but rather decreased in AITL compared with normal lymph nodes, but HEV cross-sectional area in AITL was significantly greater than that seen in normal lymph nodes. Overall, these results indicate that the prominence of AITL HEVs is likely due to increased cross-sectional area rather than increased distribution density.Entities:
Keywords: CD34; N-acetyllactosamine; sialyl Lewis x (sLex)
Mesh:
Year: 2021 PMID: 34617807 PMCID: PMC8504259 DOI: 10.1369/00221554211048551
Source DB: PubMed Journal: J Histochem Cytochem ISSN: 0022-1554 Impact factor: 4.137