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Two drugs widely used to treat certain autoimmune diseases substantially improved clinical status and reduced deaths.
Protecting the immunocompromised is not only a matter of health equity, it’s critical to ending the pandemic.
Researchers showed that B cells evolve after COVID-19 vaccination to help improve protection against SARS-CoV-2 over time.
Boosters reduced the risk of hospitalization and death by about 80% for people with HIV, cancer, autoimmune conditions or organ transplants.
Studies evaluate the impact of COVID-19 infection, treatments and vaccination in this uniquely vulnerable population.
Older and immunocompromised people and those with underlying health conditions could benefit most from additional shots.
The findings suggest boosters not only lengthen immunity but help broaden and strengthen the immune response.
People who received the Moderna COVID-19 vaccine had strong immune memory of SARS-CoV-2 six months after vaccination.
Study findings suggest that herpes simplex may trigger the development of Alzheimer’s disease, Lou Gehrig’s disease and glaucoma.
Hospital-diagnosed infections of youth between ages 11 and 19 are associated with an elevated risk of developing MS.
What protects most children from becoming seriously ill? And why does that protection sometimes fail?
About half of people hospitalized with COVID-19 had antibodies that could mistakenly attack the body’s own proteins and tissues.
Many older people have biomarkers indicative of a strong response to checkpoint inhibitors.
The booster is recommended for organ transplant recipients, people receiving cancer treatment and people with advanced or untreated HIV.
Experts call for heightened precautions and better, more intensive therapies for COVID-19 patients with weakened immune systems.
Natural immunity and vaccine responses may be weaker in people with immune suppression, so they should get their second dose promptly.
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