Advances in Cell Therapy Using Rabbit Models for Regenerative Medicine

Maria Vitória da Silva Xavier

Federal Rural University of Pernambuco, Recife-PE, Brazil.

Bruna Larissa Bernardo de Lima

Federal Rural University of Pernambuco, Recife-PE, Brazil.

José Sérgio Herculano Gomes da Silva

Federal Rural University of Pernambuco, Recife-PE, Brazil.

Elton Santos Guedes de Morais

Federal Rural University of Pernambuco, Recife-PE, Brazil.

Mariza Brandão Palma

Federal Rural University of Pernambuco, Recife-PE, Brazil.

Anísio Francisco Soares *

Federal Rural University of Pernambuco, Recife-PE, Brazil.

*Author to whom correspondence should be addressed.


Abstract

Cell therapy represents an innovative and promising approach to treating debilitating conditions, and animal testing on rabbits has played a crucial role in advancing this therapy. The objective of this manuscript aims to review the literature on the use of lagomorphs in cell therapy studies. The Pubmed and ScienceDirect databases were used, with the descriptors: Cell therapy and experimentation in rabbits; rabbits and cell therapy. After an initial retrieval of 1799 articles, those that did not specifically address the use of rabbits in cell therapy or were unrelated to the scope of this review were excluded. This resulted in a final selection of 21 articles. The present work presents a broad and distinct view of cell therapy and its different applicability, presenting a promising framework for animal experimentation in rabbits, and the advantages of using this animal model.

Keywords: Autologous therapy, allogeneic therapy, debilitating conditions, mesenchymal stem cells, tissue engineering


How to Cite

Maria Vitória da Silva Xavier, Bruna Larissa Bernardo de Lima, José Sérgio Herculano Gomes da Silva, Elton Santos Guedes de Morais, Mariza Brandão Palma, and Anísio Francisco Soares. 2024. “Advances in Cell Therapy Using Rabbit Models for Regenerative Medicine”. Archives of Current Research International 24 (10):281–286. https://doi.org/10.9734/acri/2024/v24i10931.