Guest guest Posted April 12, 2008 Report Share Posted April 12, 2008 Immunization by vaccines is a complex science. Some believe that a vaccine schedule that is too precocious can increase the risk of pathologies such as asthma in children. The following article gives credit to this theory : the vaccination history of 11,000 children in Manitoba was retrospectively studied, and it was found that children whose vaccination schedule was delayed as little as 2 months had 1/2 less occurrences of asthma. This kind of result should at the very least have the people in charge of vaccine policy in Canada do some extra research. The (crudely simplified) theory behind this is that the DPT vaccine is supposed to induce what is called a " Th2-biaised response " . This means there is an increase in the production of " T-helper-2 " lymphocytes following vaccination. T-helper lymphocytes come in 2 varieties, 1 and 2, each corresponding to a particular organization of the body's immune response. For instance, a Th1-response is more useful than a Th2-response against some viruses and bacteria, while a Th2-response is more useful against parasites. Also, both types of responses are competitive between themselves : if there is a Th-1 biais, it reduces the Th2 population, and vice-versa. The body needs and uses both types of responses according to the pathology it senses, so one is not worse or better than the other in general. For a graphic illustration of the Th1-Th2 model, see : http://www.digizyme.com/images/L3_allecure_anim.swf Problems arise when there is too much of a biais in the immune response, ie for instance when a response that should be Th1-biaised to a certain extent is not enough Th1- oriented, or when there is an over-production of Th-1 when there should not be one (and the same applies for Th-2). Vaccines may alter, briefly or more lastingly, the Th-profile, but this may vary from one vaccine to the other. For instance, some believe Pneumovaccines are more likely to induce a Th1-biaised response. Many believe asthma is a Th-2 oriented pathology, so the questioning behind the Canada study was : " Since asthma is a Th-2 disease and DTP is believed to induce a Th-2 biais, is there a possibility that vaccinating children too early might induce a Th-2 biais favorable to asthma ? " According to the article below, this causality cannot be ruled out. The Th1-Th2 theory is a model that is not perfect, but is likely to have some validity for a number of diseases. Note that it may also be partially disproved or improved in the future. Samter's is likely to be a Th2-biaised-condition (judging from Dr. son's 2006 article in the Journal of Allergy and Clinical Immunology), like asthma. Likewise, chronic rhinosinusitis with polyps is thought to be a Th2-biaised condition (see American Journal of Rhinology 2008). Would this help explain why Pneumovaccines (which may have a pro-Th1 effect) have had a temporary beneficial effect on some of us ? This is a tempting assumption. Of course, the question that springs up at this point is : if Samter's and asthma really are Th2-biaised diseases, can we shift the balance back to the normal equilibrium between Th1 and Th2, by employing something like " pro-Th1-shifters " ? Some people, including researchers, supplement manufacturers, etc have asked themselves this question and are indeed researching, producing and selling supplements, etc. At this point, however, there are more questions than answers, essentially because : - the Th1-Th2 theory is not foolproof, - the theory was designed using mice models, and it turned out that it did not work exactly in the same way in humans in a number of circumstances, - measuring the Th1-Th2 balance is not easy at all nor commonly available, so there is no possibility of knowing whether one is biaised or not, and it is likely that it will not be available soon given the cost and complexity, - even if a general Th2 biais in Samter's was proved, and supposing everyone was Th2 biaised, trying by oneself to shift a biais is not easy and probably calls for care in order not to create a biais in the other direction, - immunomudulators are sometimes safe, but also sometimes tricky meds with side effects, and their effect on the Th1-Th2 balance is rarely established (a few studies do exist, though). So, more research is warranted, as they often conclude articles. That being said, a few safe and easy things can be tried : - early sleep is associated with a Th1 profile, while late sleep is rather associated with a Th2 profile - so going to sleep early is a rather good idea for asthma and Samter's sufferers ; also, it is possible that asthmatics holding night-shift jobs experience a worsening of their condition ; - some probiotics seem to be Th1-promoters and are safe. Beta-glucans (proteins from wheat or mushrooms) seem to be Th1-promoters too, and seem safe so far, at least for short courses - but I have not researched them yet and cannot make any recommendation, and there may be a lot of differences between various brands. Here is the article about children vaccination and asthma : ------- Journal of Allergy and Clinical Immunology March, 2008 Delay in diphtheria, pertussis, tetanus vaccination is associated with a reduced risk of childhood asthma Kara L. Mc, MSca, Shamima I. Huq, BScbde, M. Lix, PhDad, Allan B. Becker, MD, FRCPCc, Anita L. Kozyrskyj, PhDabcde Received 22 September 2006; received in revised form 11 November 2007; accepted 13 November 2007. published online 21 January 2008. Background Early childhood immunizations have been viewed as promoters of asthma development by stimulating a TH2-type immune response or decreasing microbial pressure, which shifts the balance between TH1 and TH2 immunity. Objective Differing time schedules for childhood immunizations may explain the discrepant findings of an association with asthma reported in observational studies. This research was undertaken to determine whether timing of diphtheria, pertussis, tetanus (DPT) immunization has an effect on the development of childhood asthma by age 7 years. Methods This was a retrospective longitudinal study of a cohort of children born in Manitoba in 1995. The complete immunization and health care records of cohort children from birth until age 7 years were available for analysis. The adjusted odds ratio for asthma at age 7 years according to timing of DPT immunization was computed from multivariable logistic regression. Results Among 11, 531 children who received at least 4 doses of DPT, the risk of asthma was reduced to ½ in children whose first dose of DPT was delayed by more than 2 months. The likelihood of asthma in children with delays in all 3 doses was 0.39 (95% CI, 0.18-0.86). Conclusion We found a negative association between delay in administration of the first dose of whole-cell DPT immunization in childhood and the development of asthma; the association was greater with delays in all of the first 3 doses. The mechanism for this phenomenon requires further research. Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.