This section contains links to information about vaccines that was recently in the news:
Pertussis, or whooping cough, is often reported in the news when an infant dies. The disease causes severe bouts of coughing, and young infants are not physiologically or immunologically prepared to fight the infection. Because of their narrow windpipes, infants have trouble breathing during the coughing spells, sometimes turning blue; and most babies need the first three doses of pertussis vaccine to be sufficiently protected from infection. For these reasons newborns and young infants are at greater risk of hospitalization and death.
While a vaccine against pertussis has been available since the early 1900s, the history of the vaccine is complex and recently-identified strains of pertussis have made the current story more interesting.
For the purposes of this discussion, a couple of points about the biology of pertussis are important to understand:
Additional information about pertussis and the disease it causes can be found here:
The first vaccine for pertussis was made in 1914. By the late 1940s the pertussis vaccine was combined with vaccines for diphtheria and pertussis, known as the DTP vaccine. Children received three doses of DTP, with each dose separated by about one month, and a booster dose at 1 year.
The DTP vaccine contained one protein that protected against diphtheria, one protein that protected against tetanus and about 3,000 proteins that protected against pertussis. Unfortunately, the vaccine had a high rate of side effects, most of which were attributed to the pertussis component of the vaccine. Mild side effects, such as pain and swelling as well as low-grade fever, fretfulness and drowsiness occurred in one-third to one-half of children who got this vaccine. Worse, about 1 of every 100 recipients experienced persistent, inconsolable crying, 1 of every 330 had a high fever, and about 1 of every 1,750 had seizures or experienced episodes in which they became floppy (lack of muscle control) and unresponsive. While all children recovered, these side effects were scary and led researchers to work toward a better understanding of pertussis infections and development of a second, safer pertussis vaccine.
During the mid to late 1940s, pregnant women were recommended to get pertussis vaccine in an effort to protect their newborn infants with maternal antibodies.
A newer version of the pertussis vaccine became available in the 1990s. Instead of about 3,000 proteins, this acellular version contains only two to four pertussis proteins. The selected proteins are those that most commonly cause illness and allow the bacteria to infect cells in the respiratory tract. The newer version of the pertussis vaccine led to a dramatic decrease in the occurrence of side effects.
Infants and young children typically receive five doses of the vaccine known as DTaP; the first three doses, given during early infancy at 2 months, 4 months and 6 months, produce immunity. The latter two doses, typically around 15 to 18 months and again between 4 and 6 years of age, are considered booster doses – they “remind” the immune system that it has seen these disease-causing agents in the past.
Unfortunately, the medical community knew that as people got older they would become susceptible to pertussis again because the protection afforded by the vaccine given during infancy and before starting school (DTP or DTaP) was the same as the protection provided by a pertussis infection – short-term. However, the more doses of DTP or DTaP people received, the more likely they were to suffer severe (whole limb) swelling of the arm that was vaccinated. For this reason scientists designed the Tdap vaccine which contains lesser quantities of the diphtheria and pertussis vaccines; the lowercase letters in the nomenclature reflect this difference.
The Tdap vaccine is recommended for all adolescents around 11-12 years of age, and one time for adults. The exception to the recommendation for adults is that pregnant women should get the vaccine during each pregnancy, preferably during the period between 27 and 36 weeks’ gestation.
Since the acellular pertussis vaccine became available, the U.S. has experienced increases in outbreaks of pertussis. While vaccine safety concerns have caused some to forego immunizations for their children, unvaccinated children in the community are not the main reason for these outbreaks. Researchers now understand that while the acellular pertussis vaccine has a better safety profile, it is less effective. In fact, studies have shown that children who got the DTP vaccine in infancy are less likely to get pertussis than those who got the DTaP vaccine. Further, even when older adolescents and adults get the Tdap booster vaccine, the protection decreases over time.
Additionally, a group of researchers found that some strains of pertussis that are causing disease no longer contain one of the proteins contained in the vaccines, known as pertactin. Pertactin is a protein that helps bacteria adhere to cells that line the respiratory tract. Because of this finding, some have questioned whether recent pertussis outbreaks are caused by these unusual bacteria. While researchers continue to study these strains, several pieces of information are reassuring:
While these pertactin-negative strains should be monitored, they have not been found to be more dangerous than other strains of pertussis. Early data suggest pertactin-negative strains may be less virulent.
Pertussis vaccination is still the best choice for protecting ourselves and our children from pertussis. The vaccine is safe, but not perfect. Researchers should be urged to continue working toward a more effective pertussis vaccine. And, in the meantime, parents of young infants should make sure that visitors have had a Tdap booster and are not around the baby if they are ill.
Atwell JE, Van Otterloo J, Zipprich J, Winter K, Harriman K, Salmon DA, Halsey NA, Omer SB. Nonmedical vaccine exemptions and pertussis in California, 2010. Pediatrics. 2013 Oct 1; 132(4):624-30.
Baxter R, Bartlett J, Rowhani-Rahbar A, Fireman B, Klein NP. Effectiveness of pertussis vaccines for adolescents and adults: case-control study. BMJ. 2013 Jul 17;347:f4249.
Klein, N. P.; Bartlett, J.; Rowhani-Rahbar, A.; Fireman, B.; Baxter, R. Waning protection after fifth dose of acellular pertussis vaccine in children. NEJM. 2012; 367: 1012-9.
Klein NP, Bartlett J, Fireman B, Rowhani-Rahbar A, Baxter R. Comparative effectiveness of acellular versus whole-cell pertussis vaccines in teenagers. Pediatrics. 2013 Jun;131(6):e1716-22.
Queenan AM, Cassiday PK, Evangelista A. Pertactin-negative variants of Bordetella pertussis in the United States. NEJM. 2013; 368: 583-4.
By the conclusion of the holiday season, we were all hearing reports about the rampant spread of influenza across the U.S. Here’s what you should know:
Anyone can get influenza and die from it even previously healthy individuals. However, some people are at higher risk of suffering complications when they are infected with influenza:
The H1N1 strain that has been circulating tends to be particularly severe in young adults, pregnant women and obese adults.
The best protection against influenza is vaccination. Although not foolproof, getting vaccinated provides your immune system a better chance to fight infection if you are exposed:
A few antiviral medications are available to treat people infected with influenza:
Learn about the importance of getting the influenza vaccine
Meningococcus serogroup B is circulating at Princeton University and University of California Santa Barbara (UCSB). Here’s what you should know:
As of December 16, 2013:
As of January 31, 2014:
Although serogroup B meningococcal bacteria is circulating at both universities, scientists at the CDC have found that the cases at the two universities are not linked because the students were not all infected with the same strain of the bacteria.
Visit our archive page for additional information on these and other topics that were featured in previous issues of the In the News section:
Last updated: February 2014