Equally I can counteract that with this article:
pubmed.ncbi.nlm.nih.gov/27373595/
*Abstract
Background: The combination DTaP-IPV/Hib vaccine was licensed in the United States in 2008 for children ages 6weeks through 4years with doses administered at 2, 4, 6, and 15-18months of age. The aim of this study was to assess the safety of DTaP-IPV/Hib vaccine routinely administered as part of clinical care to infants at Kaiser Permanente Northern California.
Methods: This was an observational, retrospective study that included all 2-month-old infants vaccinated with either DTaP-IPV/Hib or another DTaP-containing vaccine. We monitored all subjects for non-elective hospitalizations, emergency department visits and selected outpatient outcomes (seizures, Guillain-Barré Syndrome, encephalopathy, encephalitis, alteration of consciousness, meningitis, hypersensitivity reactions, immune thrombocytopenic purpura, hemolytic anemia, type 1 diabetes, and Kawasaki disease) beginning with their first dose through 6months after a 4th dose or until 24months of age. We calculated incidence rate ratios (IRRs) in the primary analysis by comparing rates of outcomes during the post-vaccination risk interval with rates during a comparison interval more remote from vaccination. Secondary analyses compared outcomes after DTaP-IPV/Hib with those after other DTaP-containing vaccines. We reviewed the medical records of selected outcomes.
Results: From October 1, 2008 through July 31, 2010, 14,042 subjects received a first dose of DTaP-IPV/Hib, 13,194 received 2 doses, 12,548 received 3 doses and 6702 received 4 doses. Overall, there were 166 comparisons with significantly elevated IRRs and 165 comparisons with significantly reduced IRRs. Medical record review of outcomes with significantly elevated IRRs in both the primary and secondary analyses did not suggest any relationship with DTaP-IPV/Hib.
Conclusions: This study did not detect any safety concerns following DTaP-IPV/Hib and provides reassurance that DTaP-IPV/Hib administered as part of routine care was not associated with unexpected safety risks. ClinicalTrials.gov Identifier: NCT00804284.*
It does make sense that autoimmune diseases could be triggered by infections in some instances but they are not uniquely triggered by vaccines (if they are). Our bodies tend to encounter many microbes every day. Some are pathogenic and some are not and some may trigger AI in a rare number of individuals. It is very complex and whilst perhaps it may be that vaccines may trigger AI in a minority of genetically predisposed individuals I do think we should trust bodies such as JCVI to weigh up the risks and the benefits and advise when a vaccine should be given as part of a national vaccination programme. Simply stating things like this online just leads to many people deciding not to vaccinate their children with devastating consequences ( think MMR and autism scare). Personally I feel that we should trust those whose job it is to study the science and make the decisions about whether it is beneficial to vaccinate or not. Others may of course feel differently.