A new study reveals that a vaccine developed to prevent bacteria-caused diarrhea not only effectively combats Campylobacter infections but also significantly promotes faster growth in infant nonhuman primates. The HydroVax technology, also in use for other diseases, has shown promise in reducing diarrhea-associated deaths and could offer new avenues for combating infant growth stunting.
New research presents a potential solution to a bacterial infection that impacts 160 million people globally.
A new study in Nature Communications reveals that a vaccine initially created to combat bacterial diarrhea also helps infant nonhuman primates grow faster.
“The 160 million people worldwide who get sick every year from Campylobacter bacteria is far too many,” said the study’s lead researcher, Mark Slifka, Ph.D., a professor at Oregon Health & Science University’s Oregon National Primate Center. “We need a new tool to prevent bacterial diarrhea in babies and to enable more children to grow into healthy adults, and this vaccine approach looks very promising.”
The study evaluated a vaccine that uses a hydrogen peroxide-based technology called HydroVax, which Slifka developed at OHSU. The university licensed the technology to Najít Technologies, Inc., where Slifka serves as the company’s president and chief scientific officer. The technology is also helping develop vaccines against other diseases like yellow fever, West Nile, and the flu.
Campylobacter-associated diarrhea is often mild but can be fatal in young children, older adults, or people with suppressed immune systems. Although Campylobacter illness is more common in developing countries, the Centers for Disease Control and Prevention estimates that the bacteria sickens 1.5 million people in the United States every year. It is spread by consuming raw or undercooked poultry, drinking untreated water, or being in contact with animal feces.
Infant growth stunting occurs when children grow at a slower than normal pace, and may be caused by a combination of poor nutrition and repeated intestinal infections. It can lead to poor health outcomes, as well as reduced earning potential in adulthood. The World Health Organization estimates that five or more incidents of diarrhea before age 2 are the primary cause of growth stunting in a quarter of children.
Similar to what has been documented in the wild, Campylobacter naturally circulates among outdoor-housed rhesus macaques at the Oregon National Primate Research Center. Slifka and colleagues vaccinated both pregnant monkeys and their babies for this study and compared the health and growth rates of vaccinated and unvaccinated baby monkeys.
The researchers found that vaccinated baby monkeys were taller than the unvaccinated when measured from head to toe. To assess this, they specifically used LAZ, or Length-for-Age Z score, which is used to measure human children’s height relative to their age. They found the greatest difference was at 9 months of age when vaccinated monkeys had a significant LAZ improvement of 1.28. In contrast, a recent study that reviewed the outcomes of 29 clinical trials involving human infants showed that growth stunting interventions either failed to provide any significant improvement in length or, at most, provided a LAZ increase of only 0.2. Based on these comparisons, Slifka and colleagues concluded their vaccine-based approach provides a substantial improvement over what other research on infant growth stunting prevention has been able to achieve.
After receiving the first two vaccine doses, about 55% of all vaccinated baby monkeys were protected from severe diarrhea, and up to 79% were protected when both infant and mother were vaccinated. That’s a decrease from the 83% vaccine efficacy that was found in an earlier Campylobacter vaccination study of adult monkeys. Slifka said the differences may be due to changes in which Campylobacter strain is naturally circulating among the center’s nonhuman primates, and because about 80% of the infants were already infected with Campylobacter prior to their first vaccination.
Importantly, the study also found that none of the vaccinated infants contracted a lethal Campylobacter infection and that the vaccine reduced diarrhea-associated deaths for all causes — including bacteria other than Campylobacter — by 76%. This finding suggests that vaccination against this one common intestinal bacteria may also help reduce overall diarrhea-associated deaths.
“If the vaccine could be tailored to closely match the current circulating strains, administered at an earlier age, or if infants were not exposed to Campylobacter at such a young age, then there is a possibility that this vaccine approach could have even more profound effects on infant health and growth,” Slifka said.
Another interesting and unexpected finding was that infants born to vaccinated mothers had a significantly higher body mass index, or BMI, at one month of age compared with infants born to unvaccinated mothers. Because all of the adult monkeys had the same diet and all of the infants were exclusively breastfed, the researchers concluded that this result indicated vaccinating mothers during pregnancy provided an advantage to their infants at an early age. This result appears to be similar to the benefit of providing human mothers the DTaP vaccine, which provides more than 90% protection against infant whooping cough, also known as pertussis, during the first two months of life.
To build on the study’s findings, Slifka would like to explore further improving the vaccine’s effectiveness by creating a multivalent shot that fights against more than one strain of Campylobacter. Additionally, he would like to test the use of improved nutritional supplements alongside vaccination to determine if the combination further improves infant growth trajectories.
Reference: “Campylobacter vaccination reduces diarrheal disease and infant growth stunting among rhesus macaques” by Sara M. Hendrickson, Archana Thomas, Hans-Peter Raué, Kamm Prongay, Andrew J. Haertel, Nicholas S. Rhoades, Jacob F. Slifka, Lina Gao, Benjamin K. Quintel, Ian J. Amanna, Ilhem Messaoudi and Mark K. Slifka, 26 June 2023, Nature Communications.
DOI: 10.1038/s41467-023-39433-1
This work was supported by the Bill & Melinda Gates Foundation (grant INV 009576) and the National Institute of Health (grants P51 OD011092 and T32 AI007319). This publication is based on research funded in part by the Bill & Melinda Gates Foundation. The findings and conclusions contained within are those of the authors and do not necessarily reflect positions or policies of the study’s funders.
Disclosure: Mark Slifka has a significant financial interest in Najít Technologies, Inc., a company that may have a commercial interest in the results of this research and technology.
All research involving animal subjects at OHSU must be reviewed and approved by the university’s Institutional Animal Care and Use Committee (IACUC). The IACUC’s priority is to ensure the health and safety of animal research subjects. The IACUC also reviews procedures to ensure the health and safety of the people who work with the animals. No live animal work may be conducted at OHSU without IACUC approval.
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