Giunchetti, Rodolfo CordeiroSilveira, PatriciaResende, Lucilene AparecidaLeite, Jaqueline CostaMelo Júnior, Otoni Alves de OliveiraAlves, Marina Luiza RodriguesCosta, Laís MoreiraLair, Daniel FerreiraChaves, Vinícius RossiSoares, Ingrid dos SantosMendonça, Ludmila Zanandreis deLanna, Mariana FerreiraRibeiro, Helen SilvaGonçalves, Ana Alice MaiaSantos, Thaiza Aline PereiraRoatt, Bruno MendesSoares, Rodrigo Dian de Oliveira AguiarSouza, Juliana Vitoriano deMoreira, Nádia das DoresSiqueira, Fernando Augusto MathiasCardoso, Jamille Mirelle de OliveiraVital, Wendel CouraGaldino, Alexsandro SobreiraViana, Kelvinson FernandesMartins Filho, Olindo AssisLemos, Denise da SilveiraDutra, Walderez OrnelasReis, Alexandre Barbosa2020-05-082020-05-082019GIUNCHETTI, R. C. et al. Canine visceral leishmaniasis biomarkers and their employment in vaccines. Veterinary Parasitology, v. 271, p. 87-97, jul. 2019. Disponível em: <https://www.sciencedirect.com/science/article/pii/S0304401719301025>. Acesso em: 10 fev. 2020.2590-1389http://www.repositorio.ufop.br/handle/123456789/12168The natural history of canine visceral leishmaniasis (CVL) has been well described, particularly with respect to the parasite load in different tissues and immunopathological changes according to the progression of clinical forms. The biomarkers evaluated in these studies provide support for the improvement of the tools used in developing vaccines against CVL. Thus, we describe the major studies using the dog model that supplies the rationale for including different biomarkers (tissue parasitism, histopathology, hematological changes, leucocytes immunophenotyping, cytokines patterns, and in vitro co-culture systems using purified T-cells subsets and macrophages infected with L. infantum) for immunogenicity and protection evaluations in phases I and II applied to pre-clinical and clinical vaccine trials against CVL. The search for biomarkers related to resistance or susceptibility has revealed a mixed cytokine profile with a prominent proinflammatory immune response as relevant for Leishmania replication at low levels as observed in asymptomatic dogs (highlighted by high levels of IFN-γ and TNF-α and decreased levels in IL-4, TGF-β and IL-10). Furthermore, increased levels in CD4+ and CD8+ T-cell subsets, presenting intracytoplasmic proinflammatory cytokine balance, have been associated with a resistance profile against CVL. In contrast, a polyclonal B-cell expansion towards plasma cell differentiation contributes to high antibody production, which is the hallmark of symptomatic dogs associated with high susceptibility in CVL. Finally, the different studies used to analyze biomarkers have been incorporated into vaccine immunogenicity and protection evaluations. Those biomarkers identified as resistance or susceptibility markers in CVL have been used to evaluate the vaccine performance against L. infantum in a kennel trial conducted before the field trial in an area known to be endemic for visceral leishmaniasis. This rationale has been a guiding force in the testing and selection of the best vaccine candidates against CVL and provides a way for the veterinary industry to register commercial immunobiological products.en-USrestritoImmunopathologyImmunogenicityArtigo publicado em periodicohttps://www.sciencedirect.com/science/article/pii/S0304401719301025https://doi.org/10.1016/j.vetpar.2019.05.006