Søgning
Søgning på udtrykket 'cvid' giver 7 resultater
Dokumenter [3]
Sider [1]
Nyt fra tidsskrifterne [3]
Denne vejledning er tiltænkt behandling af CVID hos voksne patienter.
Den aktuelle udgave er opdateret med anvendelse af PCV20.
Denne vejledning er tiltænkt diagnostik og kontrol af CVID hos voksne patienter.
Den aktulle udgave er opdateret med PCV20.
Nyt fra tidsskrifterne [3]
Clinical & Experimental Immunology
16.10.2024
Abstract . Mutations in the human nuclear factor-κB2 gene (NFKB2) are associated with common variable immunodeficiency (CVID) or combined immunodeficiency diseases (CID), characterized by B-cell lymphopenia, hypogammaglobulinemia, and T cell dysfunction. This study investigated whether B cells with NFKB2 mutations exhibit intrinsic impairments in activation, class-switch recombination, and differentiation.
Infection
8.09.2024
the small numbers of documented cases. . . . Methods. We present a literature review and report the case of a 39-year-old female diagnosed with common variable immunodeficiency (CVID) with IgG and IgA deficiency suffering from a sepsis with L. mirabilis. As no fully closed L. mirabilis genome besides the type strain was available to date, we additionally performed complete genome sequencing of L. mirabilis. . .
Clinical & Experimental Immunology
2.05.2024
s diseases. SARS-CoV-2 vaccine has demonstrated high efficacy in preventing COVID-19 infection in the general population. However, the efficacy of this vaccine in patients with predominantly antibody deficiencies, such as common variable immunodeficiency (CVID) and X-linked agammaglobulinemia (XLA), should be closely monitored. CVID and XLA are rare genetic disorders that impair the immune system's ability to produce antibodies, which are crucial for fighting infections.