{"title":"并发粘膜和跨壁猫肠t细胞淋巴瘤表现出不同的t细胞克隆性","authors":"Masamine Takanosu , Yumiko Kagawa","doi":"10.1016/j.tvjl.2025.106361","DOIUrl":null,"url":null,"abstract":"<div><div>The clonality of 14 feline intestinal small and large T-cell lymphomas were examined, which consisted of concurrent mucosal and transmural lymphomas, respectively. Histologically, the small cell lymphomas were localized to the mucosal region and were observed adjacent to large T-cell lymphoma lesions. The large T-cell lymphomas were spread throughout the submucosal region, forming transmural lesions. Both cell types were immunohistochemically stained using anti-cluster of differentiation 3 antibody. For clonality analysis, genomic DNA was extracted from formalin-fixed, paraffin-embedded sections of the mucosal and transmural lesions, separately. Clonality analysis was performed using primer sets targeting T cell receptor beta, T cell receptor delta<em>,</em> and T cell receptor gamma loci. In 12/14 cats, the results of the clonality analysis for T-cells differed between the mucosal and transmural lesions. Despite the fact that the cellular morphologies differed between lesion types, the T-cell clonality was consistent in 1/14 cats, suggesting a common clonal origin. In the remaining case, the clonal relationship between the 2 lesions could not be determined. These results indicate that concurrent lymphomas with small and large T-cells in their mucosal and transmural lesions, respectively, develop via separate pathogenic mechanisms.</div></div>","PeriodicalId":23505,"journal":{"name":"Veterinary journal","volume":"312 ","pages":"Article 106361"},"PeriodicalIF":2.3000,"publicationDate":"2025-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Concurrent mucosal and transmural feline intestinal T-cell lymphomas show differing T-cell clonality\",\"authors\":\"Masamine Takanosu , Yumiko Kagawa\",\"doi\":\"10.1016/j.tvjl.2025.106361\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The clonality of 14 feline intestinal small and large T-cell lymphomas were examined, which consisted of concurrent mucosal and transmural lymphomas, respectively. Histologically, the small cell lymphomas were localized to the mucosal region and were observed adjacent to large T-cell lymphoma lesions. The large T-cell lymphomas were spread throughout the submucosal region, forming transmural lesions. Both cell types were immunohistochemically stained using anti-cluster of differentiation 3 antibody. For clonality analysis, genomic DNA was extracted from formalin-fixed, paraffin-embedded sections of the mucosal and transmural lesions, separately. Clonality analysis was performed using primer sets targeting T cell receptor beta, T cell receptor delta<em>,</em> and T cell receptor gamma loci. In 12/14 cats, the results of the clonality analysis for T-cells differed between the mucosal and transmural lesions. Despite the fact that the cellular morphologies differed between lesion types, the T-cell clonality was consistent in 1/14 cats, suggesting a common clonal origin. In the remaining case, the clonal relationship between the 2 lesions could not be determined. These results indicate that concurrent lymphomas with small and large T-cells in their mucosal and transmural lesions, respectively, develop via separate pathogenic mechanisms.</div></div>\",\"PeriodicalId\":23505,\"journal\":{\"name\":\"Veterinary journal\",\"volume\":\"312 \",\"pages\":\"Article 106361\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-04-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Veterinary journal\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1090023325000656\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"VETERINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Veterinary journal","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1090023325000656","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
Concurrent mucosal and transmural feline intestinal T-cell lymphomas show differing T-cell clonality
The clonality of 14 feline intestinal small and large T-cell lymphomas were examined, which consisted of concurrent mucosal and transmural lymphomas, respectively. Histologically, the small cell lymphomas were localized to the mucosal region and were observed adjacent to large T-cell lymphoma lesions. The large T-cell lymphomas were spread throughout the submucosal region, forming transmural lesions. Both cell types were immunohistochemically stained using anti-cluster of differentiation 3 antibody. For clonality analysis, genomic DNA was extracted from formalin-fixed, paraffin-embedded sections of the mucosal and transmural lesions, separately. Clonality analysis was performed using primer sets targeting T cell receptor beta, T cell receptor delta, and T cell receptor gamma loci. In 12/14 cats, the results of the clonality analysis for T-cells differed between the mucosal and transmural lesions. Despite the fact that the cellular morphologies differed between lesion types, the T-cell clonality was consistent in 1/14 cats, suggesting a common clonal origin. In the remaining case, the clonal relationship between the 2 lesions could not be determined. These results indicate that concurrent lymphomas with small and large T-cells in their mucosal and transmural lesions, respectively, develop via separate pathogenic mechanisms.
期刊介绍:
The Veterinary Journal (established 1875) publishes worldwide contributions on all aspects of veterinary science and its related subjects. It provides regular book reviews and a short communications section. The journal regularly commissions topical reviews and commentaries on features of major importance. Research areas include infectious diseases, applied biochemistry, parasitology, endocrinology, microbiology, immunology, pathology, pharmacology, physiology, molecular biology, immunogenetics, surgery, ophthalmology, dermatology and oncology.