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Peer-reviewed veterinary case report

How immune cells help canine skin histiocytoma tumors shrink

By Pires, Isabel et al.·Published in In vivo (Athens, Greece)·2013·Department of Veterinary Sciences. University of Tr&#xe1·View original on PubMed

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Original publication title: Immunohistochemical and immunoelectron study of major histocompatibility complex class-II antigen in canine cutaneous histiocytoma: its relation to tumor regression.

Species:
dog

Plain-English summary

A study looked at skin tumors called cutaneous histiocytomas in dogs to understand how their immune system helps these tumors shrink. Researchers found that all tumors showed specific markers (MHC class-II) that indicated immune activity, especially in cases where the tumors were regressing. They noticed that as the tumors shrank, there was an increase in certain immune cells (T- and B-lymphocytes) and a change in how the tumor cells displayed these markers. This suggests that the immune response plays a key role in helping these tumors to regress.

People also search for: dog skin tumor treatment · canine cutaneous histiocytoma symptoms · how to help dog with skin tumors

Abstract

In order to investigate the immune mechanisms involved in regression of canine cutaneous histicytoma (CCH), major histocompatibility complex (MHC) class-II immuno-expression and the number of T- and B-lymphocytes and macrophages were analyzed in 93 cases of CCH. MHC class-II was also studied in 16 cases of CCH by immunoelectron microscopy. All tumors expressed MHC class-II, and two major staining patterns were identified: focal juxtanuclear cytoplasmic staining and rim-like staining along the cell periphery. The MHC class-II labelling pattern and T- and B-lymphocyte infiltrates were associated with tumor regression. In regressing lesions, MHC class-II molecules shift to the cell surface and an increase of both T- and B-lymphocytes were noted. The increasing expression of MHC class-II molecules on the cell surface could be a significant factor for the onset and progression of tumour regression.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/23422487/