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Int Arch Allergy Immunol ; 183(10): 1114-1126, 2022.
Article in English | MEDLINE | ID: covidwho-1879162

ABSTRACT

Dysregulation in component 1q (C1q) levels is associated with weak placental development in preeclampsia (PE). Human immunodeficiency virus infection (HIV-1) triggers the C1q complex, resulting in opsonization of healthy host cells, contributing to their removal, and augmented progression of HIV disease. In coronavirus disease 2019 (COVID-19)-infected patients, the deposition of C1q activates the complement. Considering the paucity of data, this review highlights a significant gap in the potential of C1q in the immunocompromised state of preeclamptic HIV-infected women and COVID-19 infection. In PE, C1q is downregulated; while in antiretroviral treatment-treated HIV/COVID-19 infected patients, C1q is upregulated. It is plausible that C1q is augmented in the triad and may exacerbate severity of disease. This thereby provides a foundation for future intended research which involves the investigation of single nucleotide polymorphism expression of the C1q gene, specifically in these diseases.


Subject(s)
COVID-19 , HIV Infections , Pre-Eclampsia , Complement C1q/genetics , Complement C1q/metabolism , Complement System Proteins/metabolism , Coronavirus 3C Proteases , Female , HIV Infections/complications , HIV Infections/metabolism , Humans , Immunologic Factors/metabolism , Placenta/metabolism , Pre-Eclampsia/genetics , Pre-Eclampsia/metabolism , Pregnancy
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