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1.
Transplant Proc ; 46(10): 3371-4, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25498054

RESUMO

INTRODUCTION: Angiotensin II is a peptide hormone involved in the renin-angiotensin system (RAS). Anti-angiotensin receptor 1 (AT1R) antibodies are implicated in stimulating RAS and are suspected to have some adverse impacts on renal transplantation outcome. METHODS: From November 2009 to February 2012, 37 remaining sera from renal transplantation recipients with biopsy-proven antibody-mediated rejection (AMR) (n = 6), acute cellular rejection (ACR) (n = 23), and AMR + ACR (n = 8) without preformed human leukocyte antigeon (HLA) antibodies were tested with anti-AT1R antibody assay. Forty-two control patients without rejection also were analyzed. RESULTS: The frequency of elevated anti-AT1R antibodies was higher in patients with AMR (n = 14) compared to controls (28.6% vs 4.9%, P = .03, OR = 8.0). It was also higher in patients with AMR + ACR (n=8) (37.5% vs 4.9%, P = .03, OR = 12.0). There was no difference in frequencies of elevated anti-AT1R antibody in patients with ACR. CONCLUSION: Anti-AT1R antibodies were suspected to be associated with occurrence of AMR without preformed HLA antibodies in renal transplantation. Further studies in a larger number of patients are needed.


Assuntos
Rejeição de Enxerto/imunologia , Antígenos HLA/imunologia , Transplante de Rim , Receptor Tipo 1 de Angiotensina/imunologia , Adolescente , Adulto , Anticorpos/imunologia , Feminino , Humanos , Transplante de Rim/efeitos adversos , Masculino , Pessoa de Meia-Idade , Sistema Renina-Angiotensina , Doadores de Tecidos , Adulto Jovem
2.
Bioorg Med Chem Lett ; 8(14): 1797-800, 1998 Jul 21.
Artigo em Inglês | MEDLINE | ID: mdl-9873436

RESUMO

A series of C(7) and C(20)-substituted camptothecin derivatives (12-14, 16-18) are prepared. Their syntheses and in vitro cytotoxicities are reported.


Assuntos
Antineoplásicos/síntese química , Antineoplásicos/farmacologia , Camptotecina/análogos & derivados , Camptotecina/síntese química , Camptotecina/farmacologia , Humanos , Relação Estrutura-Atividade , Células Tumorais Cultivadas
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