Effectiveness and side effects of Moderna versus Pfizer COVID-19 vaccines
Order ID:89JHGSJE83839 Style:APA/MLA/Harvard/Chicago Pages:5-10 Instructions:
Effectiveness and side effects of Moderna versus Pfizer COVID-19 vaccines
MODERNA VERSUS PFIZER COVID-19 VACCINES
Effectiveness and side effects of Moderna versus Pfizer COVID-19 vaccines
Luis M. Cintrón Nieves
Departamento de Biología
Biol 498 Curso Integrador de Biología
October 28, 2021
Effectiveness and side effects of Moderna versus Pfizer COVID-19 vaccines
Abstract
COVID-19 has claimed many lives since it began to spread in 2020. Thanks to the efforts of science and technology, scientists were able to develop a series of vaccines to reduce its spread and negative effects. The development of these vaccines was done in record time, since a technology was known that could be capable of producing the proteins that had to be activated to fight the virus. Pfizer and Moderna developed two of these vaccines using mRNA technology. In this paper, a comparison and contrast of these vaccines is made in terms of their development, effectiveness, and side effects.
Introduction
Scientists have worked unprecedentedly to develop a vaccine to stop the spread of COVID-19, which has claimed many lives worldwide. Prior to these discoveries, prophylactic measures were recommended to control contagion through social distancing, use of masks, and frequent hand washing (Shmerling, 2021). Although these measures have been somewhat effective, it was necessary to have a drug to reduce the number of cases and deaths that were occurring on a daily basis. With the use of new technology and existing scientific knowledge, pharmaceuticals were able to alter the genetics of the virus in such a way that its mutation and resistance became more difficult. The vaccines that we currently use contain a technique known as mRNA, which causes the body to produce proteins to activate the immune system response to fight the virus (CDC, 2021). Other novel developments are currently in the testing stages, which would increase the availability of other medications to counter this virus. In this essay we are going to compare and contrast two of different types of vaccines available in terms of their formula, effectiveness and possible side effects.
Literature review
The Food and Drugs Administration (FDA) has approved the use of at least three vaccines for preventing COVID-19 contagion. Two of these vaccines are distributed by Pfizer-BioNTech and Moderna (CDC, 2021). The Pfizer-BioNTech vaccine has been approved for people over 16 years of age in two vaccines that must be given 3 weeks in between, while the vaccines for children between 5 to 15 years has an emergency use approval. On the other hand, Moderna’s vaccine can be given to people over 18 years of age in two doses 4 weeks between. With all these vaccines, immunity is supposed to be acquired after two weeks after the second dose (CDC, 2021). These means that in terms of the population that can be vaccinated, Pfizer can reach more groups within the population, including children.
In terms of the technology used to developed the vaccines both, Pfizer and Moderna used the mRNA. The mRNA technique will cause the body to produce the proteins necessary to activate the immune system against the virus (CDC, 2021). The mRNA technique, called mRNA-1273 for Moderna and BNT162b2 for Pfizer, contains encapsulated lipid nanoparticles that encode the protein that is activated by COVID-19 (Baden, et.al. 2021). These vaccines could be developed quickly by pharmaceutical companies because there was already some knowledge about mRNA for more than a decade. In the case of COVID-19, vaccines´ development only needed the correct information about the genetic sequence of the virus in order for the vaccine to be manufactured using synthetic materials. This same technology had already been proved successful in preventing influenza, Zika virus, Ebola virus, and other bacterial or parasitic infections (Maruggi, et.al., 2019).
The effectiveness of vaccines has been determined through extensive clinical studies in different groups of populations. For example, in a study with 30,420 participants it was found that mRNA technology was effective in preventing COVID-19 contagion with a 94.1% effectiveness, including in patients with severe cases and people older than 65 years old (Baden, et.al. 2021; Koff, 2021). On this matter, Nanduri et.al. (2021) found that in the nursing home population the effectiveness of Moderna’s vaccine could reach up to 92%, but with the delta variant it fell to 53.1%. In the case of the Pfizer vaccine, the level of effectiveness was estimated at 95% according to the study carried out by Polack et.al. (2020). On the other hand, the study by Kaiser et.al. (2021) found that dialysis patients who received Moderna’s vaccine had higher anti-S-antibody titers than those vaccinated with Pfizer. It can be concluded that when it comes to the effectiveness of these vaccines, both have a very similar levels, although the Pfizer vaccine the level appears to be around 3% higher.
In the first studies on the vaccines´ side effects, it was suggested that people could develop certain problems such as biodistribution and persistence of the induced immunogen expression, autoreactive antibodies, toxic effects of any non-native nucleotides or delivery system components (Wang, Kream & Stefano, 2020). However, according to the most recent literature, the most common side effects that occur from the application of these vaccines could be: pain at the injection site, pain or swelling in the lymph nodes of the arm where the vaccine was administered, fatigue, headache, muscle or joint pain, nausea and vomiting, or fever and chills, specially after the second dose (Jackson, et.at., 2021). Koff (2021) also found that these sides effects can be experimented in older adults, but in mild to moderate levels. A serious side effect that has been identified in some patients is anaphylaxis or other allergic reactions, which has occurred mainly in people who have had reactions to other vaccines in the past (Kim, et.al., 2021). These reactions occur by residual non-human proteins, preservatives or stabilizers included in the vaccines´ formula (Kim, et.al., 2021). One cannot fail to mention that these vaccines have been associated with thrombosis with thrombocytopenia deaths, but at this time they were associated with the Johnson & Johnson vaccine (See, 2021). However, this study presents the cases reported in the VAERS system and had not been peer-reviewed.
Methodology
Literature cited
Baden, L. R., El Sahly, H. M., Essink, B., Kotloff, K., Frey, S., Novak, R., Diemert, D., Spector, S. A., Rouphael, N., Creech, C. B., McGettigan, J., Khetan, S., Segall, N., Solis, J., Brosz, A., Fierro, C., Schwartz, H., Neuzil, K., Corey, L., … Zaks, T. (2021, February 4). Efficacy and safety of the mRNA-1273 SARS-COV-2 vaccine, The New England Journal of Medicine. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7787219/.
Chen, L., Zhao, J., Peng, J., Li, X., Deng, X., Geng, Z., Shen, Z., Guo, F., Zhang, Q., Jin, Y., Wang, L., & Wang, S. (2020, October 19). Detection of SARS‐CoV‐2 in saliva and characterization of oral symptoms in COVID‐19 patients.Cell Prolif. 53(12), Article e12923. https://onlinelibrary.wiley.com/doi/full/10.1111/cpr.12923.
Dooling, K., McClung, N., Chamberland, M., Marin, M., Wallace, M., Bell, B. P., Lee, G. M., Talbot, H. K., Romero, J. R., & Oliver, S. E. (2020). The Advisory Committee on Immunization Practices’ interim recommendation for allocating initial supplies of COVID-19 vaccine — United States, 2020. Morbidity and Mortality Weekly Report, 69(49), 1857–1859. https://pubmed.ncbi.nlm.nih.gov/33301429/
Gharpure, R., Patel, A., & Link-Gelles, R. (2021). First-dose COVID-19 vaccination coverage among skilled nursing facility residents and staff. Journal of the American Medical Association. 325, 1670-1671. https://pubmed.ncbi.nlm.nih.gov/33625464/
Jackson, L. A., Anderson, E. J., Rouphael, N. G., Roberts, P. C., Makhene, M., Coler, R. N., McCullough, M. P., Chappell, J. D., Denison, M. R., Stevens, L. J., Pruijssers, A. J., McDermott, A., Flach, B., Doria-Rose, N. A., Corbett, K. S., Morabito, K. M., O’Dell, S., Schmidt, S. D., Swanson, P. A., … mRNA-1273 Study Group. (2020, November 12). An mRNA vaccine against SARS-COV-2 – preliminary report. The New England Journal of Medicine. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377258/.
Jochum, S., Kirste, I., Hortsch, S., Grunert, V. P., Legault, H., Eichenlaub, U., Kashlan, B., & Pajon, R. (2021). Clinical utility of Elecsys Anti-SARS-CoV-2 S assay in COVID-19 vaccination: An exploratory analysis of the mRNA-1273 phase 1 trial. medRxiv. Article e2021.10.04.21264521 https://doi.org/10.1101/2021.10.04.21264521
Kaiser, R. A., Haller, M. C., Apfalter, P., Kerschner, H., & Cejka, D. (2021). Comparison of BNT162B2 (Pfizer–Biontech) and mRNA-1273 (Moderna) SARS-COV-2 mRNA vaccine immunogenicity in dialysis patients. Kidney International, 100(3), 697–698. https://search.bvsalud.org/global-literature-on-novel-coronavirus-2019-ncov/resource/en/covidwho-1364322
Kim, M.-A., Lee, Y. W., Kim, S. R., Kim, J.-H., Min, T. Ki., Park, H.-S., Shin, M., Ye, Y.-M., Lee, S., Lee, J., Choi, J.-H., Jang, G. C., & Chang, Y.-S. (2021). Covid-19 vaccine-associated anaphylaxis and allergic reactions: Consensus statements of the KAAACI Urticaria/Angioedema/Anaphylaxis Working Group. Allergy, Asthma & Immunology Research, 13(4), 526-544. https://doi.org/10.4168/aair.2021.13.4.526
Maruggi, G., Zhang, C., Li, J., Ulmer, J. B., & Yu, D. (2019). mRNA as a transformative technology for vaccine development to control infectious diseases. Molecular Therapy, 27(4), 757–772. https://pubmed.ncbi.nlm.nih.gov/30803823/
Nanduri, S., Pilishvili, T., Derado, G., Soe, M. M., Dollard, P., Wu, H., Li, Q., Bagchi, S., Dubendris, H., Link-Gelles, R., Jernigan, J. A., Budnitz, D., Bell, J., Benin, A., Shang, N., Edwards, J. R., Verani, J. R., & Schrag, S. J. (2021). Effectiveness of Pfizer-Biontech and Moderna vaccines in preventing SARS-COV-2 infection among nursing home residents before and during widespread circulation of the SARS-COV-2 B.1.617.2 (delta) variant — National Healthcare Safety Network, March 1–August 1, 2021. Morbidity and Mortality Weekly Report, 70(34), 1163–1166. https://doi.org/10.15585/mmwr.mm7034e3
Omar, D. I., & Hani, B. M. (2021). Attitudes and intentions towards COVID-19 vaccines and associated factors among Egyptian adults. Journal of Infection and Public Health. 2021: S1876-0341(21)00185-4. https://doi.org/10.1016/j.jiph.2021.06.019
Polack, F. P., Thomas, S. J., Kitchin, N., Absalon, J., Gurtman, A., Lockhart, S., Perez, J. L., Pérez Marc, G., Moreira, E. D., Zerbini, C., Bailey, R., Swanson, K. A., Roychoudhury, S., Koury, K., Li, P., Kalina, W. V., Cooper, D., Frenck, R. W., Hammitt, L. L., … Gruber, W. C. (2020). Safety and efficacy of the BNT162B2 mRNA Covid-19 vaccine. New England Journal of Medicine, 383(27), 2603–2615. https://doi.org/10.1056/nejmoa2034577
Spratling, R., Hallas, D. (2020). Reporting and appraising research Atudies Journal of Pediatric Health Car. 35(1), 108-113. https://www.jpedhc.org/article/S0891-5245(20)30230-3/fulltext e, 10.1016/j.pedhc.2020.08.008
Wang, F., Kream, R. M., & Stefano, G. B. (2020). An evidence-based perspective on mRNA-SARS-CoV-2 vaccine development. Medical Science Monitor, Article e924700. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7218962/
Yang, Y., Gilbert, P., Longini, Jr., I. M., & Halloran, M. E. (2008). A Bayesian framework for estimating vaccine efficacy per infectious contact. The Annals of Applied Statistics, 2(4), 1409-1431. https://doi.org/10.1214/08-aoas193
RUBRIC
Excellent Quality
95-100%
Introduction 45-41 points
The background and significance of the problem and a clear statement of the research purpose is provided. The search history is mentioned.
Literature Support
91-84 points
The background and significance of the problem and a clear statement of the research purpose is provided. The search history is mentioned.
Methodology
58-53 points
Content is well-organized with headings for each slide and bulleted lists to group related material as needed. Use of font, color, graphics, effects, etc. to enhance readability and presentation content is excellent. Length requirements of 10 slides/pages or less is met.
Average Score
50-85%
40-38 points
More depth/detail for the background and significance is needed, or the research detail is not clear. No search history information is provided.
83-76 points
Review of relevant theoretical literature is evident, but there is little integration of studies into concepts related to problem. Review is partially focused and organized. Supporting and opposing research are included. Summary of information presented is included. Conclusion may not contain a biblical integration.
52-49 points
Content is somewhat organized, but no structure is apparent. The use of font, color, graphics, effects, etc. is occasionally detracting to the presentation content. Length requirements may not be met.
Poor Quality
0-45%
37-1 points
The background and/or significance are missing. No search history information is provided.
75-1 points
Review of relevant theoretical literature is evident, but there is no integration of studies into concepts related to problem. Review is partially focused and organized. Supporting and opposing research are not included in the summary of information presented. Conclusion does not contain a biblical integration.
48-1 points
There is no clear or logical organizational structure. No logical sequence is apparent. The use of font, color, graphics, effects etc. is often detracting to the presentation content. Length requirements may not be met
You Can Also Place the Order at www.collegepaper.us/orders/ordernow or www.crucialessay.com/orders/ordernow Analyze the Water Footprint Results