Version 1
: Received: 25 July 2024 / Approved: 26 July 2024 / Online: 26 July 2024 (13:32:37 CEST)
Version 2
: Received: 30 July 2024 / Approved: 31 July 2024 / Online: 2 August 2024 (11:36:10 CEST)
Version 3
: Received: 9 October 2024 / Approved: 9 October 2024 / Online: 11 October 2024 (03:37:43 CEST)
Version 4
: Received: 11 October 2024 / Approved: 14 October 2024 / Online: 15 October 2024 (11:51:56 CEST)
Version 5
: Received: 1 November 2024 / Approved: 2 November 2024 / Online: 4 November 2024 (10:50:17 CET)
How to cite:
Carp, T.-N. Potential Innovations in Modern-Day Human and Animal Vaccine Development. Preprints2024, 2024072158. https://doi.org/10.20944/preprints202407.2158.v5
Carp, T.-N. Potential Innovations in Modern-Day Human and Animal Vaccine Development. Preprints 2024, 2024072158. https://doi.org/10.20944/preprints202407.2158.v5
Carp, T.-N. Potential Innovations in Modern-Day Human and Animal Vaccine Development. Preprints2024, 2024072158. https://doi.org/10.20944/preprints202407.2158.v5
APA Style
Carp, T. N. (2024). Potential Innovations in Modern-Day Human and Animal Vaccine Development. Preprints. https://doi.org/10.20944/preprints202407.2158.v5
Chicago/Turabian Style
Carp, T. 2024 "Potential Innovations in Modern-Day Human and Animal Vaccine Development" Preprints. https://doi.org/10.20944/preprints202407.2158.v5
Abstract
The vaccine industry has undoubtedly contributed massively in the medical world, with hundreds of millions of lives saved as a result of the successful development of prophylactic and therapeutic vaccines against various infectious and oncological diseases. Simultaneously, there has been an ongoing evolutionary battle between polymorphic microbes and the human immune system, and various microbes have developed counter-responses against the human host immune system, by creating diverse “holes” of vulnerability in the innate immune system. Such mechanisms may have resulted due to the lower prophylactic and therapeutic focus upon sharpening the innate immune lines as directly as necessary. The overall objective of vaccine-development should be the sharpening of all immune departments that are targeted by various microbial agents for the purpose of transient innate immune suppression and the distribution of the microbial count/load at a systemic level. Likewise, it could be viable for the clinical research community to start focusing upon filling in the “gaps” of vulnerability that are now present in the pathways responsible for the proper natural immune activation and proportionate signalling toward the adaptive immune system. Perhaps, through such a process, the “road” toward the adaptive immune system, which is “old” and filled with “holes”, could be gradually transformed into a perfectly uniform “highway”, with all the required signals transmitted robustly from the innate to the adaptive immune system, before microbes manage to translate the various pathogenic proteins that transiently prevent such transmission altogether, until it becomes too late for the immune response to possibly develop in a proportionate and non-harmful manner to the organism. The potential “missing piece of puzzle” in vaccine-based clinical research could involve training of the human organism to develop immune memory without the host organism reaching a threshold of clinical disease onset even if viruses translate proteins that silence the host interferon system and make it unable to trace produced toxins whilst not directly causing clinical pathophysiology. Whilst it is realistically almost impossible to train the human immune system to develop responses and memory against viral proteins that do not directly cause immunopathology, there could be a set of clinical approaches involving a stimulation for more robust activation of the host interferon system, with an example of such stimuli being the same principal elements of the interferon system. Another example of pharmaceutical approaches would involve the development of drug-like components to target such viral proteins, though they would be more costly and consequently more restricted in usage; due to the fact that viruses are obligate intracellular, particle-based parasites and can only synthesise their proteins inside host cells. Such a scenario would be possible, given that it is almost impossible for human evolutionary growth to eventually stall and not risk experiencing a decrease as a result. Simultaneously, it is important for human society to bind by the principles of maintaining a healthy and nature-friendly lifestyle, given the philosophical quote of “We are what we eat.” The overall objective should be the facilitation of human and animal immune evolution over viral and bacterial molecular self-camouflaging from all possible directions, perhaps by transferring a concept called “a United Immune System” into clinical practice, as a sharper human and animal evolutionary growth resulting from such actions could “cost” the sharper evolutionary growth of microbes as such, given that evolutionary patterns are based upon the models observed in Physics, in Newton’s Third Law of Motion, as well as in the First Law of Thermodynamics, which concerns the Conservation of Energy.
Biology and Life Sciences, Immunology and Microbiology
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.