Exploring the dynamics of IL-6, TGF-β1, and CD8+ T cells in the
canine transmissible venereal tumor: new perspectives
F Carmona Dinau1, CM González-Zambrano2, J
Jurado Jimenez3, LM Montoya Florez4*, R
Oliveira5, and N Sousa Rocha1
1Laboratory
of Investigative and Comparative Pathology, Sao Paulo State
University (UNESP), School of Veterinary Medicine and Animal
Science, Department of Veterinary Clinics, Veterinary Pathology
Laboratory, Botucatu, Brazil.2Laboratory of
Immunopathology and Infectious Agents, Sao Paulo State University
(UNESP), School of Medicine, Department of Pathology. Immunopathology
and Infectious Agents Laboratory (LIAI) Botucatu, Brazil.3Laboratory
of Investigative and Comparative Pathology, Sao Paulo State
University (UNESP), School of Medicine, Department of Pathology.
Comparative and Investigate Pathology Laboratory (LPIC) Botucatu,
Brazil.4Veterinary
Pathology Laboratory, Universidad Nacional de Colombia, School of
Veterinary Medicine, and Animal Science. Department of Animal
Health, Bogota, Colombia.5Sao Paulo State
University (UNESP), Institute of Biosciences, Department of
Biodiversity and Biostatistics, Botucatu, Brazil.
*Corresponding author:maomontoya53@yahoo.es,
lmontoyaf@unal.edu.co
Abstract
Canine transmissible venereal tumor (CTVT) serves as a valuable model for
studying tumor-immune system interactions due to its unique progression and
regression phases. This study investigated the roles of IL-6, TGF-β1, and CD8+ T
cells in CTVT progression and regression phases, evaluating their association
with therapeutic response and cytological malignancy criteria. Samples from 25
untreated dogs were analyzed via cytology, confirmed via histopathology.
Immunohistochemistry for IL-6 and TGF- β1, and CD8+ via flow cytometry. IL-6 and
TGF-β1 expression was detected in 100% of tumor samples, with cytoplasmic
localization scoring an intensity in 75% of the histological section showed
positive staining. Interestingly, IL-6 was exclusively expressed by tumor cells
in certain cases. CD8+ T cell density in tumors demonstrated a significant
negative correlation (ρ=-0.65, P<0.05) with mitotic activity, suggesting an
inverse relationship between cell proliferation and immune response. Therapeutic
response was established at the 4th week of treatment for most cases, although
some required up to ten weeks to achieve complete remission. Resistant cases
were included in a second-line chemotherapy protocol with doxorubicin,
reflecting the variability in tumor behavior. These findings propose a novel
hypothesis regarding IL-6 production by neoplastic cells as a mechanism to
suppress antigen presentation and immune activation. Further exploration of
IL-6’s dual role in tumor progression and regression may reveal potential
therapeutic targets for enhancing immune response in CTVT and other cancers.
To Cite This Article:
DinauFC, González-ZambranoCM, JimenezJJ,
FlorezLMM, Oliveir R, RochaNS, 2025.
Exploring the dynamics of IL-6, TGF-β1,
and CD8+ T cells in the canine transmissible venereal tumor: new perspectives.
Pak Vet J.
http://dx.doi.org/10.29261/pakvetj/2025.009