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IgA nephropathy, one of the most common primary glomerulonephritis worldwide, is still under investigation for its precise etiology. The widely accepted theory is the 'four-hit model' and subsequent complement and inflammatory responses. Recent studies have reported correlations between specific complement components and IgA nephropathy.

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  • Single antigen bead (SAB) assays are the main technique for detecting donor-specific HLA antibodies after a transplant, but there's a lack of direct comparisons between traditional and modified methods for better monitoring.
  • A study analyzed 251 post-transplant DSA from 91 serum samples using different treatments to determine the effectiveness of detecting antibodies; they found that some DSAs correlate with high IgG MFI values, indicating stronger antibody presence.
  • The findings suggest that both the 1:16 dilution and C1q tests are effective indicators for detecting DSAs, with C1q positively correlating with total IgG levels, and modifications to SAB assays may help refine testing and interpretation of results
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  • The study aimed to explore how COVID-19 correlates with the direct antiglobulin test (DAT) results, focusing on developing a predictive model for in-hospital mortality based on DAT types among patients with COVID-19.
  • The analysis involved 502 patients tested for DAT, revealing that those who were DAT-positive had a higher rate of confirmed COVID-19 cases and worse clinical indicators compared to DAT-negative patients.
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  • The study explores the complex immune environment in head and neck cancer (HNC) by analyzing immune cell subpopulations and their associated genes using tumor RNA sequencing data from two cohorts (192 in-house, 546 TCGA-HNSC).
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  • The research emphasizes the potential of targeting the Complement C3d Receptor 2 (CR2) gene, which is related to better tumor prognosis and stronger immune responses, suggesting that therapies focusing on CR2 could improve treatment outcomes for HNC patients.
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Inherited, age-related, and acute retinal diseases are often exacerbated by an aberrant or excessive activity of the complement system. Consequently, cells not directly affected by an acute event or genetic variants may degenerate, resulting in enhanced visual impairment. The therapeutic potential of supplementation of complement factor H (FH), a key regulator of the complement cascade, is therefore particularly promising in the context of retinal diseases caused by complement activation.

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