Evidence map›Paper›PMID 36313266›Full record

ArticleMedical hypotheses2022

Use of natural cysteine protease inhibitors in limiting SARS-Co-2 fusion into human respiratory cells.

Maciej Siewiński, Barbara Bażanów, Beata Orzechowska, Krzysztof Gołąb, Jakub Gburek, Adam Matkowski, Andrzej Rapak, Anna Janocha, Lechosław Krata, Maciej Dobrzyński and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Medical hypotheses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 85% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Maciej SiewińskiWroclaw Medical University, TherapyRaft Comp., Wroclaw, Poland.
Barbara BażanówWrocław University of Environmental and Life Sciences, Faculty of Veterinary Medicine, Department of Pathology, C.K.Norwida 31, 50-375 Wrocław, Poland.
Beata OrzechowskaLaboratory of Virology, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Weigla 12, 53-114 Wroclaw, Poland.
Krzysztof GołąbDepartment of Pharmaceutical Biochemistry, Wroclaw Medical University, Borowska 211A, Wrocław, Poland.
Jakub GburekDepartment of Pharmaceutical Biochemistry, Wroclaw Medical University, Borowska 211A, Wrocław, Poland.
Adam MatkowskiWroclaw Medical University, Dept. Pharmaceutical Biology and Biotechnology, Poland.
Andrzej RapakDepartment of Experimental Oncology, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Wroclaw, Poland.
Anna JanochaWroclaw Medical University, Dept. Physiology, Wrocław, Poland.
Lechosław KrataCovid Hospital in Walbrzych, Poland.
Maciej DobrzyńskiWroclaw Medical University, Department of Pediatric Dentistry and Preclinical Dentistry, Wroclaw, Poland.
Ewa KilarWroclaw Medical University, Dept. of Clinical Pharmacology Wroclaw, Poland.
Wroclaw Medical University · PLLudwik Hirszfeld Institute of Immunology and Experimental Therapy · PLPolish Academy of Sciences · PLWroclaw University of Environmental and Life Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Specific antibodies that humans acquire as a result of disease or after vaccination are needed to effectively suppress infection with a specific variant of SARS CoV-2 virus. The S protein of the D614G variant of coronavirus is used as an antigen in known vaccines to date. It is known that COVID-19 disease resulting from infection with this coronavirus can often be very dangerous to the health and lives of patients. In contrast, vaccines produce antibodies against an older version of the protein S-D614G (January 2020) and therefore have difficulty recognizing new variants of the virus. In our project we propose to obtain specific and precise antibodies by means of so-called controlled infection against specific infectious variants of the SARS-CoV-2 virus "here and now". Currently, several variants of this pathogen have already emerged that threaten the health and lives of patients. We propose to reduce this threat by partially, but not completely, blocking the fusion mechanism of the SARS-CoV-2 virus into human respiratory cells. According to our plan, this can be achieved by inhibiting cathepsin L activity in respiratory cells, after introducing natural and non-toxic cysteine protease inhibitors into this area. We obtain these inhibitors by our own method from natural, "human body friendly" natural resources. We hypothesize that blocking cathepsin L will reduce the number of infecting viruses in cells to such an extent that COVID-19 developing in infected individuals will not threaten their health and life. At the same time, the number of viruses will be sufficient for the body's own immune system to produce precise antibodies against a specific version of this pathogen.

Indexed as

cathepsin LControlled fusionCysteine protease 2

Identifiers

PMID36313266
PMCPMC9598048
OpenAlexW4307304092

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.