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1.
Eur J Pharm Biopharm ; 198: 114151, 2024 May.
Artigo em Inglês | MEDLINE | ID: mdl-38043622

RESUMO

Holistic concepts should be applied that reduce risks prior to final bioburden testing and sterile filtration, based on enhanced process and product attribute understanding, which could be key to successful bioburden risk management. Key findings of this paper include.


Assuntos
Biotecnologia , Filtração
2.
Crit Rev Immunol ; 37(2-6): 531-559, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29773033

RESUMO

The interleukin-1 receptor antagonist (IL-lra) is unusual in that it is the only known naturally occurring, cytokine receptor antagonist with no apparent agonist function. Over the last 5 years, since the cloning of the IL-lra cDNA sequence, there has been intensive research on the genetics, regulation, and potential therapeutic value of this protein. The later discovery of a second form of IL-lra in 1991 has complicated the picture. Whereas the originally described IL-lra is predominantly glycosylated and secreted (sIL-lra), the alternative isoform is unglycosylated and intracellular (icIL-lra). Although the biological roles of the two forms are still open to question, IL-lra is likely to be of great importance in the pathogenesis of both acute and chronic inflammatory diseases. A large body of evidence for this conclusion has come from animal models of inflammatory disease that respond well to administration of exogenous IL-lra. A role for recombinant IL-lra in the management of human disease is still under investigation. The two forms of IL-lra are encoded by a single gene by alternative usage of two first exons. Expression of sIL-lra and icIl-lra is regulated by two promoters. In this review I explore the genetics of the gene encoding IL-lra (IL-1RN) and the mechanisms of IL-lra gene activation to produce sIL-lra and icIL-lra. Also, possible biological roles for these immunomodulators in health and disease are discussed.


Assuntos
Processamento Alternativo/imunologia , Regulação da Expressão Gênica/imunologia , Inflamação/imunologia , Proteína Antagonista do Receptor de Interleucina 1/genética , Processamento Alternativo/genética , Animais , Ensaios Clínicos como Assunto , Clonagem Molecular , DNA Complementar/genética , Glicosilação , Humanos , Inflamação/tratamento farmacológico , Proteína Antagonista do Receptor de Interleucina 1/imunologia , Proteína Antagonista do Receptor de Interleucina 1/metabolismo , Proteína Antagonista do Receptor de Interleucina 1/uso terapêutico , Interleucina-1/imunologia , Interleucina-1/metabolismo , Polimorfismo Genético/imunologia , Regiões Promotoras Genéticas/genética , Isoformas de Proteínas/genética , Isoformas de Proteínas/imunologia , Isoformas de Proteínas/metabolismo , Isoformas de Proteínas/uso terapêutico , Estrutura Terciária de Proteína/genética , Receptores de Interleucina-1/imunologia , Receptores de Interleucina-1/metabolismo , Proteínas Recombinantes/genética , Proteínas Recombinantes/imunologia , Proteínas Recombinantes/metabolismo , Proteínas Recombinantes/uso terapêutico
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