key: cord-0956922-j7dn6d8o authors: Allan, Jennifer D; McMillan, Daniel; Levi, Marc L title: COVID-19 mRNA Vaccination, ABO Blood Type and the Severity of Self-Reported Reactogenicity in a Large Healthcare System: A Brief Report of a Cross-Sectional Study date: 2021-12-29 journal: Cureus DOI: 10.7759/cureus.20810 sha: adac51dbfe257243520268aa009d1806db588e33 doc_id: 956922 cord_uid: j7dn6d8o Introduction It has been anecdotally observed that ABO blood type may have an impact on the severity of the side-effects experienced by those receiving mRNA vaccination for COVID-19. Methods As part of a larger study, a retrospective cross-sectional survey was made available to approximately 33,000 front-line healthcare workers, students and volunteers who were offered voluntary vaccination in a state-wide healthcare system during phase one of the state’s vaccine roll-out. A secondary endpoint of the survey was to determine if there was any relationship between vaccination reactogenicity and ABO blood type. Results 4009 responses were received - a 12.15% response rate. 3700 respondents answered the blood type question, and of those, 2878 knew their blood type. By Kruskal-Wallis test, there was no statistically significant association between any blood type and any side effect for either of the COVID-19 mRNA vaccines. Conclusions COVID-19 mRNA vaccination may cause significant reactogenicity. However, ABO blood type does not appear to be a predictor of vaccine reactogenicity. On December 31, 2019, the World Health Organization (WHO) was first informed of a series of cases of pneumonia of unknown etiology in the city of Wuhan, China [1,2]. On February 11, 2020, the WHO officially announced that the causative agent for this novel illness was a coronavirus. The disease vector, formally named SARS-CoV-2 and the disease it causes, COVID-19, has become responsible for over 4 million deaths worldwide at the time of this writing [3] , rapidly becoming the worst public health crisis since the influenza pandemic of 1918 [4] . Messenger RNA (mRNA) vaccines for COVID-19 were introduced rapidly due in large part to existing research by National Institutes of Health staff at the Vaccine Research Center and the preparation of "prototype coronavirus vaccines" to a generic coronavirus [5] . While the development of the technology and knowhow to manufacture mRNA vaccines has been quietly progressing for many years, the public's reception of the Pfizer and Moderna vaccines for COVID-19 has been mixed due to their unfamiliarity with the technology, as well as a lack of awareness regarding both the research pathways and the side-effects of the vaccines. While significant vaccine reactogenicity was seen in preclinical trials, there was much speculation on what would account for the variation in reactogenicity seen between individuals. Shortly after mRNA COVID-19 vaccines by Pfizer [6] and Moderna [7] became available in December 2020, it was anecdotally observed that individuals of different ABO blood types appeared to experience different degrees of reactogenicity to vaccination. The frequency and severity of the reactogenicity seemed to correlate with their blood type, whereby individuals with blood type A had more severe side effects than those with blood group O. Associations between ABO blood groups and the risk of SARS-CoV-2 infection have been documented in the literature [8, 9] . The literature is very limited, however, on any relationship between vaccine reactogenicity 1 1 1 itself and the ABO blood type. Check et al published the results of a small observational study of 91 individuals where they showed a statistically significant self-reported incidence of worse vaccine reactogenicity in individuals with type A blood as compared to those with type O [10] . As part of a larger project evaluating COVID-19 vaccination and work-related absences, this project aimed to further elucidate this relationship beyond the initial anecdotal observations in a population of front-line healthcare workers employed by or working at a large, multi-site, state-wide, tertiary medical system who were offered the mRNA vaccination as part of the phase one vaccine roll-out. After Institutional Review Board review and waiver, a survey was made available to employees, healthcare providers, and volunteers of a state-wide tertiary care system through a link published in staff and medical provider electronic newsletters. Vaccination for the target population began December 14, 2020, and continued through March 2021. The retrospective data collection began on March 16, 2021, and continued through May 4, 2021. The target population was comprised of approximately 33,000 individuals with patient-facing responsibilities that made them eligible for voluntary COVID-19 vaccination with the aforementioned mRNA vaccines during the early vaccination period. Applying a cross-sectional study design, a self-reporting questionnaire (Appendices) was used to collect anonymous information. As pertaining to this secondary study objective, the questions asked included blood type, the type of vaccination received, the reactogenicity experienced, and the intensity and duration of symptoms for each injection of the two-shot mRNA vaccine. The symptoms queried were based on a modified version of the list published by the FDA on the websites describing mRNA vaccines [11, 12] . Patients reported severity on a modified Likert scale where zero indicated they did not experience the symptom and ten was considered incapacitating. A total of 4,009 responses were recorded out of approximately 33,000 eligible individuals, a 12.15% response rate. Not all respondents answered all questions. The basic demographic information of the respondents is noted in Table 1 . Of the 4,009 respondents, 3,638 reported they had received the vaccine. The side-effects reported by the vaccinated individuals, by vaccine type and scheduled vaccine are reported in Figures 1, 2. 3,700 participants answered the blood type question and 2,878 individuals knew their blood type and were vaccinated. By Kruskal-Wallis test, there was no statistically significant association between any reported blood type and any side effect for either dose of either vaccine product. The data regarding the reported side effects as stratified by blood type are reported in Tables 2, 3 . In December 2020, the CDC Advisory Committee on Immunization Practices recognized that COVID-19 vaccination was expected to elicit local and systemic reactogenicity [13] . Patient-reported adverse effects can be impacted by many factors, including age, gender, general health, ethnicity, vaccine formulation, route of administration, injection technique and individual psychological stresses ( Figure 3 ) [14] . As such, it is challenging to assess the direct impact of any individual demographic factor on the severity and duration of vaccine reactogenicity. With permission of the author [14] . ABO blood group antigens are expressed widely on cells throughout the body, and the importance of ABO membrane antigens extends beyond transfusion medicine [15] . The seroconversion to the live, attenuated influenza vaccine has been documented to be dependent on ABO blood group, whereby individuals of blood type A seroconverted after receiving a single dose, as opposed to two doses required for other ABO blood types [16] . It has also been reported that individuals with type A blood demonstrate an increased odds of COVID-19 infection while individuals with type O blood demonstrate a decreased odds of infection in [17, 18] . It would therefore seem plausible for there to be an association between ABO blood grouping and vaccine reactogenicity. As previously cited, Check et al demonstrated a statistically significant association between ABO blood group and self-reported symptom severity whereby individuals with type A blood reported more severe reactogenicity than those with blood group O [10] . Although the methodology we employed for rating severity was different from that employed by Check et al, we were unable to support their findings. While ABO blood type may have an effect on the severity of COVID-19 infection and disease, we found no statistical correlation between ABO blood type and any reactogenicity symptoms with either vaccine. This study has a number of weaknesses and limitations. The anecdotal observation that initially led to this study necessitated a retrospective data collection methodology whereby significant recall bias could be expected. Additionally, the study goals and methodology may have created a non-response/participation bias that limited the participation of individuals who did not experience reactogenicity. Finally, the sampling method, which relied on emailed newsletters, biased the respondent sample to those who opened the email and read the newsletters. This sampling bias, as well as the preponderance of nurses responding, may account for the overwhelming number of female respondents and those who describe their job type as "other." Local and systemic reactogenicity are known and expected occurrences after the Pfizer and Moderna mRNA COVID-19 vaccinations and are seen in a considerable percentage of those surveyed. Although ABO blood type appears to be associated with COVID-19 disease severity, we found no connection between ABO blood type and vaccine reactogenicity with mRNA vaccines. Due to the timing of this study, we were unable to ascertain if a relationship exists between blood type and reactogenicity for other types of vaccines, specifically the Janssen/Johnson & Johnson vaccine, which uses a viral vector. Further research into this area is warranted. If you didn't opt to receive the vaccine, please tell us briefly why you have chosen not to be vaccinated: Human subjects: Consent was obtained or waived by all participants in this study. Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work. A Novel Coronavirus from Patients with Pneumonia in China Global Public Health Database Support to Population-Based Management of Pandemics and Global Public Health Crises, Part I: The Concept Fast, reliable, universal: corbett recounts quest for covid vaccine . 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