Mod-E-RNA, cancers and Programmed cell Death Protein 1 pathway (PD-1/PD-L1). And who is Len Blavatnik?
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Updates first, the main post is under the divider bar.
Update 4/4/2024: What are the PD-1 inhibitors which block the receptors on tumor cells? Flavonoids, as simple as cabbage in a daily diet….
Update: 3/17/2024: despite of their crimes, Mod-E-RNA expands: https://expose-news.com/2024/03/17/why-is-moderna-substantially-expanding-manufacturing-capacity-despite-current-low-demand-for-their-poison/ . Who is paying for this global universal annihilation of the human genome?? US???
Update 3/3/2024: reminder of an old issue, in 2012 filed Moderna patent for “METHODS AND COMPOSITIONS FOR TARGETING AGENTS INTO AND ACROSS THE BLOOD-BRAIN BARRIER“ at https://patents.justia.com/patent/20150030576 specifically states, that “modified mRNAs that are capable of penetrating the blood-brain barrier (BBB) for delivery to the central nervous system (CNS)” and “The modified nucleic acids or mmRNA of the invention may include a first region of linked nucleosides encoding a polypeptide of interest, a first flanking region located at the 5′ terminus of the first region, and a second flanking region located at the 3′ terminus of the first region.” and that mmRNA can be a modified uridine, like N1-methyl-pseudouridine, the one from covid genetically modifying injections. That means, COVID INJECTIONS WERE DESIGNED ON PURPOSE TO CROSS BBB!!! Incorporation can happen via 2 ways, electrical currents or soundwaves.
Update 2/29/2024: Anti cancer treatments with IV of liposomal p53 gene, IVs of VITC, blood ozone treatments, propolis applications, all of which have direct killing effect on cancer cells, according to Dr. Akiyama from Tokyo (TTAC info). Other example from Japan to use plain water fasting, for 12 days, in order to get rid of cancer.
Update 1/7/2024: new links to more generous support of Mr. Blavatnik, DARPA related (thanks to https://forbiddenknowledgetv.net/leave-the-world-behind-sonic-weapon-explained/), at the end of this post.
Update 1/9/24: Blavatnik School Of Government https://www.bsg.ox.ac.uk/research/covid-19-government-response-tracker
The physical feeling of an empty space, like a desert, or a food store in a communist land, with nothing in it but the sales person, is just a moment of surprise, or not even that, when you look at the faces of those who wanted democracy, wrong, freedom (Tiananmen square, 1989, video on Ytube lXJ6gHFME0w):
A missing person in ones life, generates a different empty space around, no matter how full, or empty it is… That space is in the heart. And a smile on a humans face, suddenly can fill up that space again. A good healthy soul and spirit always fills that space, in a time independent way. That’s the ‘forever thing’ in which the death of something much bigger than matter, has no place. That physical death is feared most, and that’s what CIA lives from, fear. And it propagates into all ‘intelligence’, in particular science.
The ‘modern science’ claims that the Cell Death on a molecular level is associated with few major proteins, among others, one is called PD-L1, which stands for Programmed cell Death Ligand 1, a protein with features summarized at https://www.uniprot.org/uniprotkb/Q9NZQ7/entry . And the other is called PD-1, Programmed cell Death protein 1, with more details on it at https://www.uniprot.org/uniprotkb/Q15116/entry. Both proteins play an important role in apoptosis, cell death and thus in cancer cure (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7136921/). Few of those examples from uniprot data base:
PD-1 is inhibiting immune responses and promoting self-tolerance through modulating the activity of T-cells.
Delivers inhibitory signals upon binding to ligands CD274/CD273
PD-1 associates with CD3-TCR in the immunological synapse and directly inhibits T-cell activation
Blocking the PD-1/PD-L1 pathway will affect the immune response. Anti–PD-1/PD-L1 treatments, according to the recent Mod-E-RNA clinical trials of their new NEO-anti-gen anti-cancer vaccines https://s29.q4cdn.com/435878511/files/doc_presentations/2023/Apr/16/aacr-23_ct001-mrna4157_april-16.pdf , will need monitoring of just one factor (p. 13), the PD-L1 status:
“mRNA-4157 (V940) and pembrolizumab combination treatment demonstrated an improvement in RFS irrespective of PD-L1 status”, where RFS stands for relapse-free survival. The PD-1/PD-L1 pathway as a target in Mod-E-RNA cancer treatment, https://investors.modernatx.com/news/news-details/2023/Merck-and-Moderna-Initiate-Phase-3-Study-Evaluating-V940-mRNA-4157-in-Combination-with-KEYTRUDA-pembrolizumab-for-Adjuvant-Treatment-of-Patients-with-Resected-High-Risk-Stage-IIB-IV-Melanoma/default.aspx was very predictable, given that PD-1, an inhibitory receptor on antigen activated T-cells, plays a critical role in induction and maintenance of immune tolerance to self. Following T-cell receptor (TCR) engagement, PD-1 directly inhibits T-cell activation. It suppresses T-cell activation through the recruitment of PTPN11/SHP-2: following ligand-binding, PD-1 is phosphorylated within the ITSM motif, leading to the recruitment of the tyrosine phosphatase PTPN11/SHP-2 that mediates dephosphorylation of key TCR proximal signaling molecules, such as ZAP70, PRKCQ/PKCtheta and CD247/CD3zeta. With one word, tolerance and autoimmunity are connected^1 and T-cells are essential in this process^2.
The VAERS system, tracing side effects of covid genetically modifying injections, as of 11-18-2022 has stopped putting free text field information in the public data for Europe/UK (https://www.openvaers.com/covid-data). So based on what’s left there, Moderna COVID-19 (mRNA-1273) injections and their bivalent followers caused, according to VAERS (run in expert mode) 779 cases of all sorts of autoimmune conditions including 10 deaths. That, despite of the global suppression or straight prohibition (like in Kaiser Permanente facilities, surely just one out of many) to enter the covid injections injuries into VAERS, by the ‘oversight’. It does not include a family member, who suddenly got ‘citric acid’ allergy, yes, the same from the TCA cycle of every human of earth..!??
It gets even stranger, because the cancer/carcinoma cases AFTER Mod-E-RNA injections registered in VAERS are:
“Found 28 cases where Vaccine is COVID19 or COVID19-2 and Manufacturer is MODERNA and Symptom is Cancer fatigue or Cancer gene carrier or Cancer in remission or Cancer pain or Cancer screening or Cancer screening normal or Cancer staging or Cancer surgery”, with NOT A ONE DEATH.
I personally have a neighbor, who died after the 3-rd Mod-E-RNA shot due to super fast growing liver/lung cancer, another friend who died Jan ‘23 after the 4th, due to heart issues, another one, just 2 weeks ago, and countless others who developed cancers or suffered re-emissions shortly after… And I’m just one out here, seeing the damage, VAERS can’t see…
So now, Mod-E-RNA, which managed to inject billions(?) with the highest (~3x the amount in Pfizer’s BNT162b2 ) concentration of synthetic genetic material of NON-HUMAN, patented origin, has their new computer based construct stitched out of ~34 mod mRNA Neo-Antigen pieces as a personalized anti-cancer mod mRNA GENETIC MODIFICATION TREATMENT, which ‘they’ still call ‘vaccine’. That one method, out of 5 others, mRNA-4157 PCV (Merck) has the following mode of action:
whereby the application of a specific drug called pembrolizumab, according to: https://s29.q4cdn.com/435878511/files/doc_presentations/2023/Apr/16/aacr-23_ct001-mrna4157_april-16.pdf , results in a ‘great outcome’, quote from p.14: “mRNA-4157, a personalized cancer vaccine, in combination with pembrolizumab, demonstrates trend for improved recurrence free survival compared to pembrolizumab alone in adjuvant melanoma patients across tumor mutational burden subgroups”. Never mind the table from p.11, listing 104 cases of significant adverse events in 104 tested patients…
What is pembrolizumab? It is human IgG4 (mutant S228P) anti-PD1 antibody with a 3D structure known for almost a decade: https://www.rcsb.org/structure/5DK3.
Surely everyone remembers the headlines from last year:
”IgG4 Antibodies Induced by Repeated Vaccination May Generate Immune Tolerance to the SARS-CoV-2 Spike Protein” https://pubmed.ncbi.nlm.nih.gov/37243095/
“IgG4-related Disease Emerging after COVID-19 mRNA Vaccination” https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10258086/
“Post-COVID mRNA-vaccine IgG4 shift: worrisome?” https://pubmed.ncbi.nlm.nih.gov/37191589/
Sounds like that’s the same human IGg4 in Moderna’s new drug ‘wonder’ and the one associated with the Spike gene based treatments.… What if we take the heavy chain from IGg4 of that 5DK3 pembrolizumab structure and compare it to the Spike bound to ‘UT28K-RD Fab heavy chain|Homo sapiens’ from the 8K5H Pdb data bank in the “Structure of the SARS-CoV-2 BA.1 spike with UT28-RD”? BLAST gives even in the default mode, no twitching, 92% sequence coverage with 77% IDENTITY. Here the major one, with query being part of Spike anti-body, and Sbjct the ‘anti-cancer-antibody’ PD-1:
292 bits(748) 3e-102 Compositional matrix adjust. 171/223(77%) 188/223(84%) 2/223(0%)
Query 1 QMQLVQSGPEVKKPGTSVKVSCKASGFRFSISAVQWVRQARGQRLEWIGWIVVGSGDTNY
Q+QLVQSG EVKKPG SVKVSCKASG+ F+ + WVRQA GQ LEW+G I +G TN+
Sbjct 1 QVQLVQSGVEVKKPGASVKVSCKASGYTFTNYYMYWVRQAPGQGLEWMGGINPSNGGTNF
Query 61 AQKFQERVTITRDMSTSTAYMELSSLRFEDTAVYYCAAPYCGGDCSDGFDIWGQGTMVTV
+KF+ RVT+T D ST+TAYMEL SL+F+DTAVYYCA D GFD WGQGT VTV
Sbjct 61 NEKFKNRVTLTTDSSTTTAYMELKSLQFDDTAVYYCARRDYRFDM--GFDYWGQGTTVTV
Query 121 SSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQ
SSASTKGPSVFPLAP S+STS TAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQ
Sbjct 119 SSASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQ
Query 181 SSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPK 223
SSGLYSLSSVVTVPSSSLGT+TY CNV+HKPSNTKVDK+VE K
Sbjct 179 SSGLYSLSSVVTVPSSSLGTKTYTCNVDHKPSNTKVDKRVESK 221
an for the light chain of anti-Spike and human IgG4 (mutant S228P) anti-PD1 antibody, it looks even better:
390 bits(1001) 2e-144 Compositional matrix adjust. 195/218(89%) 200/218(91%) 3/218(1%)
Query 21 EIVLTQSPGTLSLSPGERATLSCRASQSVSSS---YLAWYQQKPGQAPRLLIYGASSRAT
EIVLTQSP TLSLSPGERATLSCRAS+ VS+S YL WYQQKPGQAPRLLIY AS +
Sbjct 1 EIVLTQSPATLSLSPGERATLSCRASKGVSTSGYSYLHWYQQKPGQAPRLLIYLASYLES
Query 78 GIPDRFSGSGSGTDFTLTISRLEPEDFAVYYCQQYGNSPWTFGQGTKVEIKRTVAAPSVF
G+P RFSGSGSGTDFTLTIS LEPEDFAVYYCQ + P TFG GTKVEIKRTVAAPSVF
Sbjct 61 GVPARFSGSGSGTDFTLTISSLEPEDFAVYYCQHSRDLPLTFGGGTKVEIKRTVAAPSVF
Query 138 IFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLS
IFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLS
Sbjct 121 IFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLS
Query 198 STLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 235
STLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC
Sbjct 181 STLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 218
Doesn’t it look like the Moderna ‘Spike vaccines’ prepared the victims for their ‘anti-cancer’ new ‘wonder’ treatment with 100% significant adverse events, similarly to what the covid injections did? Anyone, who reads this and is familiar with immune ‘therapies’, please help out here, I’m just looking at the amino acid sequences…
Thus clearly Spike must be somewhat related to the Programmable Death Proteins and their ligands, that PD-1/PD-L1 pathway. According to uniprot, PD-1 has 2 conserved negatively charged motifs (just few amino acids long!!):
PD-1’s immunoreceptor tyrosine-based inhibitory motif (ITIM): VDYGEL (221-226)
PD-1’s immunoreceptor tyrosine-based switch motif (ITSM) : EYATI (247-251)
inside of the full length PD-1 protein with the sequence code Q15116.3 (PD-1 in Query line). The comparison with SARS-CoV-2 Spike (also called Spike2020 for the first version of it) shows ~27% of identities (SARS-CoV-2 Spike code YP_009724390.1), among others the following homologous sections, including the above ITIM and ITSM motifs:
Query 18 GWRPGWFLDSPDRPWNPPTFSPALLVVTEGDNATF-TCSFSNTSESFVLNWY 68 PD1
GW G LDS + +LL+V N C F ++ F+ +Y
Sbjct 103 GWIFGTTLDSK---------TQSLLIVNNATNVVIKVCEFQFCNDPFLGVYY 145
Query 56 FSNT-SESFVL--NWYRMSPSNQTDKLAAF----PED 85 PD-1
F+N ++SFV+ + R QT K+A + P+D
Sbjct 392 FTNVYADSFVIRGDEVRQIAPGQTGKIADYNYKLPDD 428 Spike2020
Query 26 DSPDRPWNPPTFSPALLVVTEGDNATFTCSFSNTSES 62 PD-1
D+P P+N + TE N F T +S
Sbjct 80 DNPVLPFNDGVY----FASTEKSNIIRGWIFGTTLDS 112 Spike2020
by hand the section which
>>VDYGEL<<=ITIM motif !!!
Query 207 QPLKEDPSAVPVFSVDYGELDFQWREKTPEPPVP PD-1
Q +K+ + P+ D+G F++ + P+P P
Sbjct 784 Q-VKQIYKTPPIK--DFGG--FNFSQILPDPSKP Spike2020
Tyr789 * <<phosphorylated
BLAST determined sections with switch motif 'EYATI':
Query 246 TEYAT-IVFPSGMGTS 260 PD-1
++Y++ ++ G TS
Sbjct 871 AQYTSALLA--GTITS 885 Spike2020
Query 238 PVPCVPEQTEYATIVF 251 PD-1
+ C +Y++ F
Sbjct 746 STECSNLLLQYGS--FCT 759 Spike2020
Query 247 EYATIVFPSGMG 258 PD-1
EY + F +
Sbjct 169 EYVSQPFLMDLE 180 Spike2020
Query 221 VDYGELDFQWREKTPEPPVPCVPEQTEYA 249 PD-1
VD+ +++ +P V + Y
Sbjct 1040 VDFCGKGYHLMSFPQSAPHGVVFLHVTYV 1068 Spike2020
Query 247 EYATIV 252 PD-1
+++ V
Sbjct 428 DFTGCV 433 Spike2020
Query 241 CV-PEQTEYATIVFP 251 PD-1
C P Q+ Y+
Sbjct 488 CYFPLQS-YG---FQPTN 496 Spike2020
BLAST cant find that one, so by hand, FULL COVERAGE
CVPEQTEYATIVFPSG-M PD-1
CV ++Y+ +++ S +
CV---ADYS-VLYNSASF Spike2020
CVPEQ----TE-YATIVFPS-GM-GT PD-1
K-PFERDISTEIYQAGSTPCNGVEGF Spike2020 - ACE2 receptor binding domain
Also the richest Trp section, as conserved in the HIV gp160 protein is here:
QA-PWPV-VWAVLQLGWRPGWFLD PD-1
QYIKWPWYIWLGFIAGLIAIVMVT Spike2020
All of the above, does not look random, to me.
According to this summary titled “Clinical and Recent Patents Applications of PD-1/PD-L1 Targeting Immunotherapy in Cancer Treatment—Current Progress, Strategy, and Future Perspective “ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358377/ the number of patents related to PD-1/PD-L1 pathway started to explode around 2015, despite of the Nobel-prize winning discovery of PD-1 in 1992:
and the top FDA ‘approved’ were:
from which the mentioned pembrolizumab has the application for the widest range of all sorts of cancers (Table 4). That’s where Mod-E-RNA comes in. In 2015 it signed agreement with MERCK to develop mRNA-based anti-viral vaccines, after it developed the synthetic mod mRNA doing even better job than the natural mRNA version. It was with 2013 DARPA’s financial support when the RNA ‘therapeutics’ started its progress (https://www.flagshippioneering.com/timelines/moderna-timeline The ModERNA collaboration with Harvard however, was way before the official admission, that on September 26th, 2019 Harvard University establishes mRNA immunotherapy research collaboration with Moderna.
The 2 big names in the CRISP/RNA genetics/PD-1/PD-L1 arena, all going back to Moderna, are linked to the Blavatnik Institute (BI). The Blavatnik Family Foundation has made sizable investments into Harvard University, the New York Academy of Sciences, Oxford University, and other institutions, in total ~$900 million. Much of Harvard’s Office of Technology Development success has come from the life sciences, where commercially promising research can get an extra boost from the Blavatnik Biomedical Accelerator, and where emerging companies benefit from Boston’s robust early-stage venture ecosystem. These 2 mentioned BI members are:
Dr. George Church, covid19 national response team
Dr. Arlene Sharpe, The Blavatnik Biomedical Accelerator Advisory Committee (https://otd.harvard.edu/accelerators/blavatnik-biomedical-accelerator/), holder of every Harvard patent for PD-1 related molecules.
Blavatnik, Ukrainian-born British-American businessman and philanthropist., with apparently no ties to Russia any more, pays for the TOP geneticist George Church, for lot of work at MIT, for others in Yale (https://medicine.yale.edu/news-article/blavatnik-family-foundation-to-provide-10-million-grant-for-immunobiology-research-at-yale/ , https://ventures.yale.edu/news/blavatnik-fund-innovation-yale-awards-25-million-11-yale-faculty-led-projects-developing-new) , Columbia (https://www.engineering.columbia.edu/news/blavatnik-gift), for scientists from all over (https://www.eurekalert.org/news-releases/709174), who are lucky to be supported by such a generous rich source, to a level, where even CNN gets concerned, since when equally, LOT of politicians, including the honorable EDGE member Bill, everyone knows (picture from https://edition.cnn.com/2022/05/11/us/russian-oligarchs-philanthropy-ukraine-war-invs/index.html),
all are getting lot of money, the question is, where it comes from and is its purpose really a pure philanthropy? Certainly, politics does not belong to that category, by definition. The https://hms.harvard.edu/research/blavatnik-institute with a special department at https://sysbio.med.harvard.edu/about-our-faculty and research areas at: http://be.mit.edu/research-areas/systems-biology has one more special member of the EDGE.org society:
http://be.mit.edu/directory/laurie-a-boyer, a MODERNA Consultant 2016-2020 and then in 2018, just on time, received a grant in: “Regenerative medicine holds great promise for treating heart failure, but that promise is unrealized, in part, due to a lack of sufficient understanding of heart development at the mechanistic level. Boyer’s research aims to achieve a deep, mechanistic understanding of the gene control switches that coordinate normal heart development. She then aims to leverage this knowledge and design effective strategies for rewiring faulty circuits in aging and disease.” (https://news.mit.edu/2018/advancing-knowledge-medical-genetic-sciences-mathers-foundation-grants-0626). It could be just coincidence, after all each human has just one heart, which can get sick, for many reasons. Just the timing is strange…
The official list of money spend by Blavatnik for BOTH political 2-party system in USA at:
https://www.opensecrets.org/donor-lookup/results?name=blavatnik&order=desc&sort=A
and his company with countless biotechnology investments:
https://www.accessindustries.com/
smells like insider trader on almost all the issues which the covid gene based therapies are causing, from blood related heme synthesis modulation (https://www.discmedicine.com/our-pipeline/), to cancer treatments, in particular children ( https://www.dayonebio.com/), iron storage, including the PD-1/PD-L1 pathway. Blavatnik’s influence on science, politics, economy (https://www.thedailybeast.com/len-blavatnik-and-his-access-industries-are-shareholders-of-calpine-which-helped-kill-clean-energy-in-maine) but science in particular (https://sysbio.med.harvard.edu/about-our-faculty) is indeed stunning!
Only few people in this world get that far as Len Blavatnik did, the position of a https://en.wikipedia.org/wiki/Knight_Bachelor in 2017, which maybe ended with https://www.royal.uk/the-order-of-the-garter, all this after opening in 2010, the Blavatnik School of Government at Oxford University. That all in turn proceeded the big money flow for MIT (~200mln$ in 2018).
Len Blavatnik also extensively supports research done in Israel, in particular one of the top scientific research centers in the world, the Weizman Institute established by Chaim Azriel Weizmann (https://en.wikipedia.org/wiki/Chaim_Weizmann, the Russian-born biochemist, Zionist leader and Israeli statesman who served as a president of the Zionist Organization and later became the first president of Israel):
In fact, the entire scientific-advisory-council of Blavatnik’s Institute gives awards to only 3 nations, US, UK and Israel:
http://blavatnikawards.org/awards/national-awards/
http://blavatnikawards.org/awards/united-kingdom-awards/
http://blavatnikawards.org/awards/israel-awards/scientific-advisory-council/
The amount of money involved in private sectors and general research in genetics can be found here:
https://frontlinegenomics.com/world-of-genomics-usa/
https://frontlinegenomics.com/world-of-genomics-israel/
and some of the planned future here:
https://d4-pharma.com/the-festival-of-genomics-biodata-in-london-2024/
Last thought:
Is the Russiagate ‘scandal’ a programmed cell death from very begin? Who knows:
https://qz.com/1521847/major-gop-donor-len-blavatnik-had-business-ties-to-a-russian-official
I’m very sorry for citing wiki too often. Looks like wiki-leaks has quite a lot on Blavatnik too: https://search.wikileaks.org/?q=Len+Blavatnik
Now the newest, related to financing different areas of Mr. Blavatnik interests.
An ultrasonic analysis of the new B+M Obama’s movie called ‘Leave the world behind’ presented by Bonnie and John Mitchell of AwakenVideo^3 points to an applications of DARPA’s technology developed under a project within the Brain Initiative (https://www.darpa.mil/program/our-research/darpa-and-the-brain-initiative). The project’s name is Electrical Prescriptions (ElectRx). Two researchers involved in ElectRx who are mentioned at https://www.darpa.mil//news-events/2015-10-05 were also financially supported by Blavatnik:
Dr. Elisa Konofagou (Columbia) (https://www.engineering.columbia.edu/news/latest%20blavatnik%20fellows%20announced)
Polina Anikeeva, PhD (MIT) (http://blavatnikawards.org/news/items/announcing-finalists-2020-blavatnik-national-awards-young-scientists/)
It looks like the ‘Self-Healing of Body and Mind’ as advertised by DARPA in its project, was used in Obama’s movie (!!) in an extremely evil way, to actually harm the viewers^3. It is hard to imagine the involved scientists know about who and how is using their work. The Michell family mentions in their presentation a very new science field, the s.c. sonogenetics, which when combined with optogenetics, can remotely stimulate the human body in an unprecedented way.
And lastly, this post is NOT to condemn science, which lives from finances, and maybe that’s why it is so limited, but rather to point to the fact, that every work everyone is doing is paid by somebody with special interests, and those can be good, or bad. Always keeping an eye on who is doing what with ones own work, should be kept in mind, while judging upon anyone but oneself..
Thank you for the attention, and
Belated Happy New Year Wishes!
Literature.
Ian R Mackay “Tolerance and autoimmunity”. West J Med. 2001 Feb; 174(2): 118–123. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1071274/
Prabhakaran Kumar et al. “Restoring self-tolerance in autoimmune diseases by enhancing regulatory T-cells“ Cell Immunol. 2019 May:339:41-49. https://pubmed.ncbi.nlm.nih.gov/30482489/
https://forbiddenknowledgetv.net/leave-the-world-behind-sonic-weapon-explained/
The 'm' messenger in mRNA = Messianic
Goød told me that; pray into Genesis 50:20.