Excerpt:

Firstly, “Detection of recombinant Spike protein in the blood of individuals vaccinated against SARS-CoV-2: Possible molecular mechanisms” (Wiley Online Library, 2023.08.31). The Jab-manufactured (recombinant) S spike protein differs from the virial infection-produced (natural) S spike in that the recombinant S spike contains two proline substitutions to “stabilize the S spike in the open configuration”, as they say. So, the study tested for the manufactured PP-Spike in the serum of post-jab subjects and in the serum of unvaccinated infected subjects. None of the unvaccinated infected subjects were tested positive for PP-Spike. The kicker: 50% of the “vaccinated” subject tested positive for the PP-Spike, for 69 to whopping 187 days after the jab.

Hence my title of this post: the good news is that 50% of “vaccinated” subjects possibly received a “placebo” with non-functional mRNA; the bad news is, the other 50% became long-term S-spike generating machines. How is this possible? Only two ways, according to the study authors: either the mRNA code gets imbedded in your cells’ DNA, or in the DNA of the bacteria that you permanently host. Either way, you have a lasting (or permanent?) fountain of PP-Spike inside of you.

In their own words:

Experimental design: Mass spectrometry examination of biological samples was used to detect the presence of specific fragments of recombinant Spike protein in subjects who received mRNA-based vaccines.

Results: The specific PP-Spike fragment was found in 50% of the biological samples analyzed, and its presence was independent of the SARS-CoV-2 IgG antibody titer. The minimum and maximum time at which PP-Spike was detected after vaccination was 69 and 187 days, respectively.

Graphs

According to the authors [15] and in general, the vaccine messenger RNA nanoparticle molecules should be picked up by the immune cells in the lymph nodes after injection into the muscle. Recently, other authors have isolated vaccine messenger RNA sequences from peripheral plasma after 28 days after injection [24]. The question of whether or not the vaccine RNA can be integrated into the lymphocyte or other body cells is much debated. Nonetheless, the observation of the protein produced, as presented in this manuscript, goes beyond the purely cognitive aspect and defines a method to verify not only the persistence of the vaccine RNA but the quantification of the product, that is, the protein that is supposed to induce antibody production, in order to verify the correct half-life and a possible need to update the vaccine status. Using mass spectrometry examination of biological samples, we detected the presence of specific fragments of recombinant Spike protein in about 50% of subjects who received mRNA-based vaccines. In some cases, we found the PP-Spike marker in vaccinated individuals more than 30 days after the vaccine, indicating that it is possible to detect vaccine “Spike” protein even sometime after vaccination and in any organic tissue (data in preparation). Based on the results obtained, hypotheses can be made for possible molecular mechanisms of persistence of “Spike PP.” In particular, three hypotheses are possible and are shown in Figure 3.

It is possible that the mRNA may be integrated or re-transcribed in some cells.

It is possible that pseudo-uridines at a particular sequence position, as described in the article, induce the formation of a spike protein that is always constitutively active. But it seems very remote as a hypothesis.

It is possible that the mRNA-containing nanoparticle will be picked up by bacteria normally present at the basal level in the blood. In fact, the existence of blood microbiota in clinically healthy individuals was proven during the last 50 years. Indeed, indirect evidence by radiometric analyses suggested the existence of living microbial forms in erythrocytes [25]. In addition, the observation of the PP-Spike marker in individuals vaccinated more than 30 days after the vaccine in about 50% of subjects could also be explained by the wide biodiversity of eukaryotic and prokaryotic microbiota identified in blood by next-generation sequencing technologies [25].

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The OP goes on to examine two more recent studies.

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The inflammation markers clearly show ongoing inflammation after a jab (1st or 2nd), highest within 30 days post 2nd jab, returning to normal (unjabbed) levels only after 180 days or so.

To add some context, myocardial FDG uptake on PET/CT is an established diagnostic technique to actually see where (which organs of your body) the inflammation is ongoing (here, here, here).

Long story short, 50% of the Covid-19 jab mRNA-injected subject for sure have myocardial and other endothelial inflammation for the duration of PP S spike production in their bodies, which is up to more than half a year on end.