Scientists reassess how to treat babies born to HIV-infected mothers

After HIV is detected in Mississippi baby thought to be cured, researchers look beyond antiretroviral prophylaxis

In light of the recent news that HIV has been detected in the Mississippi baby previously thought to have been cured of the disease, researchers are assessing how to help those born to HIV-infected mothers. These infants around the world are in need of new immune-based protective strategies, including vaccines delivered to mothers and babies and the means to boost potentially protective maternal antibodies, said researchers reporting in the Cell Press journal Trends in Microbiology.

Sally Permar, MD, PhD "There is a real need for additional HIV-1 prevention methods for infants," said Dr. Sallie Permar, Assistant Professor in Pediatrics, Immunology, Molecular Genetics and Microbiology at the Duke University Medical Center Human Vaccine Institute.

A misperception exists that infant HIV-1 infection is no longer a problem due to the known efficacy of antiretroviral prophylaxis. However, the pediatric HIV-1 epidemic is not close to being over, with more than 250,000 infants infected last year. We must work towards developing novel HIV-1 prophylaxis strategies that are safe, easy to administer, and effective, allowing every child a chance for a healthy life.

Almost half of the children infected with HIV-1 are born healthy but then contract the virus through their mother's breast milk. Formula feeding is recommended to HIV-infected mothers in developed countries, but limited access to clean water and formula in addition to the known health benefits of breast milk often make breastfeeding the best option for parents in other parts of the world, despite the HIV risk.

Many women in developing countries also struggle with access to antiretroviral therapies. According the United Nations program on HIV/AIDS, in 2012 only 62 percent of identified HIV-infected pregnant women received optimal antiretroviral therapy for the prevention of mother-to-child transmission during pregnancy, and even fewer (49 percent) received antiretroviral therapy during breastfeeding.

Timing of potential immune-based interventions to prevent postnatal HIV-1 infections (Source: Fouda et al, Trends in Microbiology)Fortunately, only 10 percent of breastfed infants born to HIV-1-infected women acquire the virus, despite prolonged exposure, the researchers report, perhaps because of maternal and infant immune factors that scientists, including Dr. Permar's group, are only now beginning to identify and understand. If the efficacy of those antiviral factors can be confirmed, they might form the basis for new HIV-preventive nutritional supplements or immunity-boosting therapies, the report's authors said.

Recent advances have also been made in HIV vaccines delivered to adults, and Dr. Permar said it will now be critical to test their use in children. Although additional research in both animals and humans is needed, she and her colleagues are optimistic that gains in reducing the incidence of HIV-1 infection among infants will continue.

"I believe there is great hope that a generation free of HIV-1 can be achieved, as we have achieved less than two percent mother-to-child HIV transmission in the US," she said. "However, recent data has indicated that antiretroviral prophylaxis alone may not be adequate to achieve this goal globally. "The first adult HIV-1 vaccine trial that demonstrated vaccine efficacy was reported in 2009, and we are optimistic that a similar or improved vaccine could protect infants as well and synergize with current antiretroviral prophylaxis to eliminate pediatric HIV-1 infections."

Read the article

This article is freely available for two weeks until August 13, 2014:

Fouda et al: "Immune-based interventions to prevent postnatal HIV-1 transmission," Trends in Microbiology.


Elsevier Connect Contributor

Mary Beth O'LearyMary Beth O'Leary (@MaryBethPress) is Press Officer for Cell Press(@CellPressNews), based in Cambridge, Massachusetts. She began her career at Cell Press as an Senior Editorial Assistant for the journal Cell before transitioning into the marketing/media relations department. As Press Officer, she works closely with the media on communicating the scientific breakthroughs published in Cell Press's 30 journals to the public. A graduate of the College of the Holy Cross in Worcester, Massachusetts, she studied literature and art history.

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