Human cytomegalovirus (HCMV) is widespread and usually causes no symptoms in healthy people, but it can harm organ transplant recipients, cancer patients and newborns. The CDC calls HCMV the most infectious cause of birth defects in the United States, and congenital infection affects up to 2% of pregnancies worldwide. Some estimates put global infection rates above 80%.
HCMV makes viral Fc receptors (vFcγRs) that bind antibodies and stop them from activating immune cells such as natural killer (NK) cells. A team led by researchers at the University of Texas at Austin engineered IgG1 antibodies with altered regions so the virus cannot bind them. The antibodies still trigger NK cells and, in lab tests, blocked spread between cells and reduced viral dissemination in infected cultures.
Coauthors include scientists at UT Austin, Cardiff University’s School of Medicine and the University of Freiburg. Researchers are testing combinations with antiviral drugs or vaccines, and they say more testing is needed before clinical use.
Difficult words
- cytomegalovirus — a common virus that can cause serious infections
- congenital — present at birth or before birth
- antibody — a protein the immune system makes to fight germsantibodies
- immune — relating to the body's system that fights infection
- receptor — a protein on cells that binds specific moleculesreceptors
- engineer — to design or change something for a purposeengineered
- dissemination — the process of spreading something widely
Tip: hover, focus or tap highlighted words in the article to see quick definitions while you read or listen.
Discussion questions
- How could engineered antibodies help people at high risk from HCMV?
- Why do you think researchers want more testing before clinical use?
- Would you feel confident using a new antibody treatment after lab tests? Why or why not?
Related articles
Drug‑resistant Salmonella in children’s food and water in Karamoja
A peer‑reviewed study found drug‑resistant Salmonella in nearly half of food and water consumed by under‑fives in Karamoja. High resistance to azithromycin and other drugs raises health, economic and development concerns.
Gut has a backup system for IgA antibodies
Researchers found two different routes that make IgA antibodies in the gut. Early IgA often comes from non‑germinal center cells but later from germinal centers; both types showed similar specificity and mutations, which may help vaccine design.