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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Regulatory T cells counteract neuropathic pain through inhibition of the Th1 response at the site of peripheral nerve injury

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Autor(es):
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Davoli-Ferreira, Marcela [1, 2] ; de Lima, Kalil A. [1, 2, 3] ; Fonseca, Miriam M. [1, 4] ; Guimaraes, Rafaela M. [1] ; Gomes, I, Francisco ; Cavallini, Maria C. [5, 2] ; Quadros, Andreza U. [5] ; Kusuda, Ricardo [5] ; Cunha, Fernando Q. [5] ; Alves-Filho, Jose C. [5] ; Cunha, Thiago M. [5]
Número total de Autores: 11
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Ctr Res Inflammatory Dis CRID, Ribeirao Preto Med Sch, Dept Pharmacol, Ribeirao Preto, SP - Brazil
[2] Univ Sao Paulo, Sch Med Ribeirao Preto, Grad Program Basic & Appl Immunol, Ribeirao Preto - Brazil
[3] Univ Virginia, Ctr Brain Immunol & Glia BIG, Dept Neurosci, Charlottesville, VA - USA
[4] Wake Forest Sch Med, Dept Anesthesiol, Pain Mech Lab, Winston Salem, NC 27101 - USA
[5] Gomes, Francisco, I, Univ Sao Paulo, Ctr Res Inflammatory Dis CRID, Ribeirao Preto Med Sch, Dept Pharmacol, Ribeirao Preto, SP - Brazil
Número total de Afiliações: 5
Tipo de documento: Artigo Científico
Fonte: Pain; v. 161, n. 8, p. 1730-1743, AUG 2020.
Citações Web of Science: 0
Resumo

The inflammatory/immune response at the site of peripheral nerve injury participates in the pathophysiology of neuropathic pain. Nevertheless, little is known about the local regulatory mechanisms underlying peripheral nerve injury that counteracts the development of pain. Here, we investigated the contribution of regulatory T (Treg) cells to the development of neuropathic pain by using a partial sciatic nerve ligation model in mice. We showed that Treg cells infiltrate and proliferate in the site of peripheral nerve injury. Local Treg cells suppressed the development of neuropathic pain mainly through the inhibition of the CD4(+)Th1 response. Treg cells also indirectly reduced neuronal damage and neuroinflammation at the level of the sensory ganglia. Finally, we identified IL-10 signaling as an intrinsic mechanism by which Treg cells counteract neuropathic pain development. These results revealed Treg cells as important inhibitory modulators of the immune response at the site of peripheral nerve injury that restrains the development of neuropathic pain. In conclusion, the boosting of Treg cell function/activity might be explored as a possible interventional approach to reduce neuropathic pain development after peripheral nerve damage. (AU)

Processo FAPESP: 13/08216-2 - CPDI - Centro de Pesquisa em Doenças Inflamatórias
Beneficiário:Fernando de Queiroz Cunha
Modalidade de apoio: Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs
Processo FAPESP: 11/19670-0 - Mecanismos envolvidos na fisiopatologia da artrite reumatóide, dor e sepse
Beneficiário:Fernando de Queiroz Cunha
Modalidade de apoio: Auxílio à Pesquisa - Temático