Internal Medicine Department, Ecole Nationale Vétérinaire d'Alfort, Maisons-Alfort, France.
Laboratory of Cellular and Molecular Mechanisms of Hematological Disorders and Therapeutical Implications, INSERM U1163, Imagine Institute, Paris, France.
Lab Invest. 2021 Jun;101(6):794-804. doi: 10.1038/s41374-021-00581-x. Epub 2021 Mar 10.
Indolent T cell lymphoproliferative disorder (LPD) of the gastrointestinal tract (GI-TLPD) is a rare human primary gastrointestinal T cell lymphoma that was recently included in the 2016 revision of the World Health Organization classification of lymphoid neoplasms. Low-grade intestinal T cell lymphoma (LGITL), an emerging disease in the domestic cat, shares a number of features with human GI-TLPD. In this prospective study, we determined whether feline LGITL might serve as a model of human GI-TLPD. We analyzed clinical, laboratory, and radiological data and performed histopathological and molecular studies on small intestinal biopsies from 22 domestic cats diagnosed with LGITL. This cancer mostly affects aging cats, is associated with nonspecific gastrointestinal tract signs, and is usually characterized by an indolent course. A histopathological analysis indicated that LGITL was mainly located in the jejunum. The small intestinal lamina propria was infiltrated by large numbers of small CD3+ T cell lymphocytes with various CD4 and CD8 expression profiles (CD4+ CD8- (4 out of 11, 36%), CD4- CD8+ (3 out of 11, 27%), and CD4- CD8- (4 out of 11, 36%)). Intraepithelial lymphocyte (IEL) counts were elevated in all cases. Ki67 was expressed in lamina propria lymphocytes and IELs at a low level (<30%). Most LGITLs were labelled by antibodies against phosphorylated STAT5, but were negative for CD56 and phosphorylated STAT3. T cell receptor gamma chain gene monoclonality was found in 86% of cases. These findings confirmed that feline LGITL shares clinical and histopathological features with human GI-TLPD. Feline LGITL may therefore constitute a relevant model of the human disease.
惰性 T 细胞淋巴增生性疾病(LPD)是一种罕见的人类原发性胃肠道 T 细胞淋巴瘤,最近被纳入 2016 年世界卫生组织淋巴肿瘤分类的修订版。低级别肠道 T 细胞淋巴瘤(LGITL)是一种在国内猫中新兴的疾病,与人类 GI-TLPD 具有许多共同特征。在这项前瞻性研究中,我们确定了猫 LGITL 是否可能成为人类 GI-TLPD 的模型。我们分析了 22 只被诊断患有 LGITL 的家猫的临床、实验室和放射学数据,并对小肠活检进行了组织病理学和分子研究。这种癌症主要影响老年猫,与非特异性胃肠道症状有关,通常表现为惰性病程。组织病理学分析表明,LGITL 主要位于空肠。小肠固有层被大量具有不同 CD4 和 CD8 表达谱的小 CD3+T 细胞淋巴细胞浸润(11 例中有 4 例,占 36%,CD4+CD8-;3 例,占 27%,CD4-CD8+;4 例,占 36%,CD4-CD8-)。所有病例的上皮内淋巴细胞(IEL)计数均升高。Ki67 在固有层淋巴细胞和 IEL 中低表达(<30%)。大多数 LGITL 被针对磷酸化 STAT5 的抗体标记,但对 CD56 和磷酸化 STAT3 呈阴性。86%的病例发现 T 细胞受体γ链基因单克隆性。这些发现证实了猫 LGITL 与人类 GI-TLPD 具有临床和组织病理学特征。因此,猫 LGITL 可能构成人类疾病的相关模型。