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  1. Article ; Online: Atypical B cells are part of an alternative lineage of B cells that participates in responses to vaccination and infection in humans.

    Sutton, Henry J / Aye, Racheal / Idris, Azza H / Vistein, Rachel / Nduati, Eunice / Kai, Oscar / Mwacharo, Jedida / Li, Xi / Gao, Xin / Andrews, T Daniel / Koutsakos, Marios / Nguyen, Thi H O / Nekrasov, Maxim / Milburn, Peter / Eltahla, Auda / Berry, Andrea A / Kc, Natasha / Chakravarty, Sumana / Sim, B Kim Lee /
    Wheatley, Adam K / Kent, Stephen J / Hoffman, Stephen L / Lyke, Kirsten E / Bejon, Philip / Luciani, Fabio / Kedzierska, Katherine / Seder, Robert A / Ndungu, Francis M / Cockburn, Ian A

    Cell reports

    2021  Volume 34, Issue 6, Page(s) 108684

    Abstract: The diversity of circulating human B cells is unknown. We use single-cell RNA sequencing (RNA-seq ... to examine the diversity of both antigen-specific and total B cells in healthy subjects and malaria-exposed ... individuals. This reveals two B cell lineages: a classical lineage of activated and resting memory B cells and ...

    Abstract The diversity of circulating human B cells is unknown. We use single-cell RNA sequencing (RNA-seq) to examine the diversity of both antigen-specific and total B cells in healthy subjects and malaria-exposed individuals. This reveals two B cell lineages: a classical lineage of activated and resting memory B cells and an alternative lineage, which includes previously described atypical B cells. Although atypical B cells have previously been associated with disease states, the alternative lineage is common in healthy controls, as well as malaria-exposed individuals. We further track Plasmodium-specific B cells after malaria vaccination in naive volunteers. We find that alternative lineage cells are primed after the initial immunization and respond to booster doses. However, alternative lineage cells develop an atypical phenotype with repeated boosts. The data highlight that atypical cells are part of a wider alternative lineage of B cells that are a normal component of healthy immune responses.
    MeSH term(s) Adult ; Antibodies, Protozoan/immunology ; B-Lymphocytes/immunology ; Child ; Child, Preschool ; Female ; Humans ; Malaria/immunology ; Malaria/prevention & control ; Malaria Vaccines/administration & dosage ; Malaria Vaccines/immunology ; Male ; Plasmodium/immunology ; RNA-Seq ; Vaccination
    Chemical Substances Antibodies, Protozoan ; Malaria Vaccines
    Language English
    Publishing date 2021-02-10
    Publishing country United States
    Document type Clinical Trial, Phase III ; Journal Article ; Multicenter Study ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2020.108684
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Reduced Binding between Omicron B.1.1.529 and the Human ACE2 Receptor in a Surrogate Virus Neutralization Test for SARS-CoV-2.

    Hoffman, Tove / Kolstad, Linda / Akaberi, Dario / Järhult, Josef D / Rönnberg, Bengt / Lundkvist, Åke

    Viruses

    2023  Volume 15, Issue 6

    Abstract: ... angiotensin-converting enzyme 2 (hACE2) receptor and the spike (S) protein of the Wuhan, Delta, and Omicron (B ... regarding qualitative results. Binding between the hACE2 receptor and the S1 domain of the B.1.1.529 lineage ... the receptor binding domain (RBD) in a reduced manner, suggesting less efficient receptor binding for the B.1.1 ...

    Abstract The current gold standard assay for detecting neutralizing antibodies (NAbs) against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the conventional virus neutralization test (cVNT), which requires infectious virus and a biosafety level 3 laboratory. Here, we report the development of a SARS-CoV-2 surrogate virus neutralization test (sVNT) that, with Luminex technology, detects NAbs. The assay was designed to mimic the virus-host interaction and is based on antibody blockage between the human angiotensin-converting enzyme 2 (hACE2) receptor and the spike (S) protein of the Wuhan, Delta, and Omicron (B.1.1.529) variants of SARS-CoV-2. The sVNT proved to have a 100% correlation with a SARS-CoV-2 cVNT regarding qualitative results. Binding between the hACE2 receptor and the S1 domain of the B.1.1.529 lineage of the Omicron variant was not observed in the assay but between the receptor and an S1 + S2 trimer and the receptor binding domain (RBD) in a reduced manner, suggesting less efficient receptor binding for the B.1.1.529 Omicron variant. The results indicate that the SARS-CoV-2 sVNT is a suitable tool for both the research community and the public health service, as it may serve as an efficient diagnostic alternative to the cVNT.
    MeSH term(s) Humans ; Neutralization Tests ; Angiotensin-Converting Enzyme 2 ; SARS-CoV-2/genetics ; COVID-19/diagnosis ; Antibodies, Neutralizing ; Spike Glycoprotein, Coronavirus/genetics ; Antibodies, Viral
    Chemical Substances Angiotensin-Converting Enzyme 2 (EC 3.4.17.23) ; Antibodies, Neutralizing ; Spike Glycoprotein, Coronavirus ; Antibodies, Viral ; spike protein, SARS-CoV-2
    Language English
    Publishing date 2023-05-30
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2516098-9
    ISSN 1999-4915 ; 1999-4915
    ISSN (online) 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v15061280
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Deer mastadenovirus B pneumonia in a white-tailed deer fawn.

    Hoskins, Emily / Hoffman, Jay / Ferro, Pamela J / Diaz-Delgado, Josué / Porter, Brian F / Gomez, Gabriel / Cliften, Paul

    Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc

    2023  Volume 35, Issue 5, Page(s) 543–546

    Abstract: A 7-mo-old farmed white-tailed deer fawn ( ...

    Abstract A 7-mo-old farmed white-tailed deer fawn (
    MeSH term(s) Cattle ; Animals ; Deer ; Mastadenovirus/genetics ; Adenoviridae Infections/veterinary ; Pneumonia/veterinary ; Cattle Diseases
    Language English
    Publishing date 2023-06-12
    Publishing country United States
    Document type Journal Article
    ZDB-ID 287603-6
    ISSN 1943-4936 ; 1040-6387
    ISSN (online) 1943-4936
    ISSN 1040-6387
    DOI 10.1177/10406387231179140
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Mutations in topoisomerase IIβ result in a B cell immunodeficiency.

    Broderick, Lori / Yost, Shawn / Li, Dong / McGeough, Matthew D / Booshehri, Laela M / Guaderrama, Marisela / Brydges, Susannah D / Kucharova, Karolina / Patel, Niraj C / Harr, Margaret / Hakonarson, Hakon / Zackai, Elaine / Cowell, Ian G / Austin, Caroline A / Hügle, Boris / Gebauer, Corinna / Zhang, Jianguo / Xu, Xun / Wang, Jian /
    Croker, Ben A / Frazer, Kelly A / Putnam, Christopher D / Hoffman, Hal M

    Nature communications

    2019  Volume 10, Issue 1, Page(s) 3644

    Abstract: B cell development is a highly regulated process involving multiple differentiation steps ... yet many details regarding this pathway remain unknown. Sequencing of patients with B cell-restricted ... previously known role in B cell development. We use Saccharomyces cerevisiae, and knockin and knockout murine ...

    Abstract B cell development is a highly regulated process involving multiple differentiation steps, yet many details regarding this pathway remain unknown. Sequencing of patients with B cell-restricted immunodeficiency reveals autosomal dominant mutations in TOP2B. TOP2B encodes a type II topoisomerase, an essential gene required to alleviate topological stress during DNA replication and gene transcription, with no previously known role in B cell development. We use Saccharomyces cerevisiae, and knockin and knockout murine models, to demonstrate that patient mutations in TOP2B have a dominant negative effect on enzyme function, resulting in defective proliferation, survival of B-2 cells, causing a block in B cell development, and impair humoral function in response to immunization.
    MeSH term(s) Animals ; B-Lymphocytes/immunology ; Cell Differentiation ; DNA Topoisomerases, Type II/genetics ; DNA Topoisomerases, Type II/immunology ; Female ; Humans ; Male ; Mice ; Mice, Knockout ; Mutation ; Primary Immunodeficiency Diseases/enzymology ; Primary Immunodeficiency Diseases/genetics ; Primary Immunodeficiency Diseases/immunology ; Primary Immunodeficiency Diseases/physiopathology ; Saccharomyces cerevisiae/cytology ; Saccharomyces cerevisiae/enzymology ; Saccharomyces cerevisiae/genetics
    Chemical Substances DNA Topoisomerases, Type II (EC 5.99.1.3)
    Language English
    Publishing date 2019-08-13
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-019-11570-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Polymer Architecture Effects on Poly(N,N-Diethyl Acrylamide)-b-Poly(Ethylene Glycol)-b-Poly(N,N-Diethyl Acrylamide) Thermoreversible Gels and Their Evaluation as a Healthcare Material.

    Haddow, Peter J / da Silva, Marcelo A / Kaldybekov, Daulet B / Dreiss, Cecile A / Hoffman, Ewelina / Hutter, Victoria / Khutoryanskiy, Vitaliy V / Kirton, Stewart B / Mahmoudi, Najet / McAuley, William J / Cook, Michael T

    Macromolecular bioscience

    2021  Volume 22, Issue 3, Page(s) e2100432

    Abstract: ... PDEA-b-poly(ethylene glycol) (PEG)-b-PDEA are synthesized to give four block copolymers with varied ... on PDEA (20 kDa)-b-PEG (10 kDa)-b-PDEA (20 kDa) is designed by optimizing the polymer concentration and ... architecture on the nanostructure and rheology of PDEA-b-PEG-b-PDEA and presents the development of a highly ...

    Abstract Thermoreversible gels which transition between liquid-like and solid-like states when warmed have enabled significant novel healthcare technologies. Poly(N,N-diethyl acrylamide) (PDEA) is a thermoresponsive polymer which can be used as a trigger to form thermoreversible gels, however its use in these materials is limited and crucial design principles are unknown. Herein ABA copolymers with the structure PDEA-b-poly(ethylene glycol) (PEG)-b-PDEA are synthesized to give four block copolymers with varied molecular weight of PDEA and PEG blocks. Rheometry on solutions of the block copolymers reveals that high molecular weight PEG blocks are required to form thermoreversible gels with predominantly solid-like behavior. Furthermore, small-angle X-ray scattering elucidates clear differences in the nanostructure of the copolymer library which can be linked to distinct rheological behaviors. A thermoreversible gel formulation based on PDEA (20 kDa)-b-PEG (10 kDa)-b-PDEA (20 kDa) is designed by optimizing the polymer concentration and ionic strength. It is found that the gel is mucoadhesive, stable, and non-toxic, as well as giving controlled release of a hydrophobic drug. Overall, this study provides insight into the effect of polymer architecture on the nanostructure and rheology of PDEA-b-PEG-b-PDEA and presents the development of a highly functional thermoreversible gel with high promise for healthcare applications.
    MeSH term(s) Acrylamide ; Delivery of Health Care ; Gels/chemistry ; Hydrogels/chemistry ; Polyethylene Glycols/chemistry ; Polymers/chemistry ; Temperature
    Chemical Substances Gels ; Hydrogels ; Polymers ; Acrylamide (20R035KLCI) ; Polyethylene Glycols (3WJQ0SDW1A)
    Language English
    Publishing date 2021-12-11
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2039130-4
    ISSN 1616-5195 ; 1616-5187
    ISSN (online) 1616-5195
    ISSN 1616-5187
    DOI 10.1002/mabi.202100432
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Atypical B cells are part of an alternative lineage of B cells that participates in responses to vaccination and infection in humans

    Henry J. Sutton / Racheal Aye / Azza H. Idris / Rachel Vistein / Eunice Nduati / Oscar Kai / Jedida Mwacharo / Xi Li / Xin Gao / T. Daniel Andrews / Marios Koutsakos / Thi H.O. Nguyen / Maxim Nekrasov / Peter Milburn / Auda Eltahla / Andrea A. Berry / Natasha KC / Sumana Chakravarty / B. Kim Lee Sim /
    Adam K. Wheatley / Stephen J. Kent / Stephen L. Hoffman / Kirsten E. Lyke / Philip Bejon / Fabio Luciani / Katherine Kedzierska / Robert A. Seder / Francis M. Ndungu / Ian A. Cockburn

    Cell Reports, Vol 34, Iss 6, Pp 108684- (2021)

    2021  

    Abstract: Summary: The diversity of circulating human B cells is unknown. We use single-cell RNA sequencing ... RNA-seq) to examine the diversity of both antigen-specific and total B cells in healthy subjects and ... malaria-exposed individuals. This reveals two B cell lineages: a classical lineage of activated and ...

    Abstract Summary: The diversity of circulating human B cells is unknown. We use single-cell RNA sequencing (RNA-seq) to examine the diversity of both antigen-specific and total B cells in healthy subjects and malaria-exposed individuals. This reveals two B cell lineages: a classical lineage of activated and resting memory B cells and an alternative lineage, which includes previously described atypical B cells. Although atypical B cells have previously been associated with disease states, the alternative lineage is common in healthy controls, as well as malaria-exposed individuals. We further track Plasmodium-specific B cells after malaria vaccination in naive volunteers. We find that alternative lineage cells are primed after the initial immunization and respond to booster doses. However, alternative lineage cells develop an atypical phenotype with repeated boosts. The data highlight that atypical cells are part of a wider alternative lineage of B cells that are a normal component of healthy immune responses.
    Keywords B cell memory ; atypical B cells ; alternative B cell lineage ; malaria ; sporozoite ; vaccination ; Biology (General) ; QH301-705.5
    Subject code 610
    Language English
    Publishing date 2021-02-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Cathepsin B p.Gly284Val Variant in Parkinson's Disease Pathogenesis.

    Milanowski, Lukasz M / Hou, Xu / Bredenberg, Jenny M / Fiesel, Fabienne C / Cocker, Liam T / Soto-Beasley, Alexandra I / Walton, Ronald L / Strongosky, Audrey J / Faroqi, Ayman H / Barcikowska, Maria / Boczarska-Jedynak, Magdalena / Dulski, Jaroslaw / Fedoryshyn, Lyuda / Janik, Piotr / Potulska-Chromik, Anna / Karpinsky, Katherine / Krygowska-Wajs, Anna / Lynch, Tim / Olszewska, Diana A /
    Opala, Grzegorz / Pulyk, Aleksander / Rektorova, Irena / Sanotsky, Yanosh / Siuda, Joanna / Widlak, Mariusz / Slawek, Jaroslaw / Rudzinska-Bar, Monika / Uitti, Ryan / Figura, Monika / Szlufik, Stanislaw / Rzonca-Niewczas, Sylwia / Podgorska, Elzbieta / McLean, Pamela J / Koziorowski, Dariusz / Ross, Owen A / Hoffman-Zacharska, Dorota / Springer, Wolfdieter / Wszolek, Zbigniew K

    International journal of molecular sciences

    2022  Volume 23, Issue 13

    Abstract: ... affected siblings and to subsequently assess the role of mutations in Cathepsin B ...

    Abstract Parkinson's disease (PD) is generally considered a sporadic disorder, but a strong genetic background is often found. The aim of this study was to identify the underlying genetic cause of PD in two affected siblings and to subsequently assess the role of mutations in Cathepsin B
    MeSH term(s) Cathepsin B/genetics ; Cathepsin B/metabolism ; Genotype ; Heterozygote ; Humans ; Parkinson Disease/genetics ; Penetrance
    Chemical Substances CTSB protein, human (EC 3.4.22.1) ; Cathepsin B (EC 3.4.22.1)
    Language English
    Publishing date 2022-06-25
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms23137086
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Deer mastadenovirus B pneumonia in a white-tailed deer fawn

    Hoskins, Emily / Hoffman, Jay / Ferro, Pamela J. / Diaz-Delgado, Josué / Porter, Brian F. / Gómez, Gabriel / Cliften, Paul

    Journal of Veterinary Diagnostic Investigation. 2023 Sept., v. 35, no. 5 p.543-546

    2023  

    Abstract: ... for genome sequence analysis, which revealed a 99.6% match to Deer mastadenovirus B (formerly Odocoileus adenovirus 2 ...

    Abstract A 7-mo-old farmed white-tailed deer fawn (Odocoileus virginianus) died after several weeks of progressive deterioration associated with endoparasitism and respiratory signs. A field autopsy was performed, and lung tissue was submitted for histologic examination. The findings were consistent with necrosuppurative bronchointerstitial pneumonia with intranuclear viral inclusions. Immunofluorescence using fluorescently labeled polyclonal antibodies to bovine adenovirus 3 and 5 was positive. To rule out cross-reactivity with other adenoviruses, formalin-fixed, paraffin-embedded tissue sections were submitted for genome sequence analysis, which revealed a 99.6% match to Deer mastadenovirus B (formerly Odocoileus adenovirus 2, OdAdV2). To our knowledge, natural clinical disease associated with OdAdV2 has not been reported previously.
    Keywords Bovine mastadenovirus B ; Odocoileus virginianus ; cross reaction ; fawns ; fluorescent antibody technique ; histology ; lungs ; necropsy ; nucleotide sequences ; pneumonia ; sequence analysis ; Adenoviridae ; Deer mastadenovirus B ; bovine adenovirus 3 ; bronchointerstitial pneumonia ; Cervidae ; immunofluorescence ; white-tailed deer
    Language English
    Dates of publication 2023-09
    Size p. 543-546.
    Publishing place SAGE Publications
    Document type Article ; Online
    ZDB-ID 287603-6
    ISSN 1943-4936 ; 1040-6387
    ISSN (online) 1943-4936
    ISSN 1040-6387
    DOI 10.1177/10406387231179140
    Database NAL-Catalogue (AGRICOLA)

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  9. Article ; Online: Clonal expansion and markers of directed mutation of IGHV4-34 B cells in plasmablasts during Kawasaki disease.

    Chang, Arthur J / Baron, Sarah / Hoffman, Jonathon / Hicar, Mark D

    Molecular immunology

    2022  Volume 145, Page(s) 67–77

    Abstract: ... of the coronary arteries, a superantigen response, and a post-infectious autoimmune phenomenon. A role for B cell ... responses during KD are supported by numerous findings including B cell specific markers identified ...

    Abstract Kawasaki disease (KD) is the leading cause of acquired heart disease in children. The cause remains unknown; however, epidemiologic and demographic data support a single preceding infectious agent may lead to KD. A variety of pathophysiologic responses have been proposed, including direct invasion of the coronary arteries, a superantigen response, and a post-infectious autoimmune phenomenon. A role for B cell responses during KD are supported by numerous findings including B cell specific markers identified in genome wide association studies. We have recently published data showing children with KD have similar plasmablast (PB) responses to children with infections. Since during other infections, cells expressing antibodies against the preceding infection are enriched in PBs, we sought to explore the specific antibodies encoded by PBs during KD. In one child we see a massive expansion in IGHV4-34 utilizing antibodies, which has been associated with autoimmunity in the past. We further explored this expansion of IGHV4-34 utilization during the peripheral PB rise with next generation sequencing (NGS) analysis and utilizing newer techniques of chromium chip single cell separation (10x Genomics®). We also utilized peptide array screening to attempt to identify an antigen to the most prolific clones.
    MeSH term(s) Antibodies/genetics ; B-Lymphocytes ; Biomarkers ; Child ; Genome-Wide Association Study ; Humans ; Mucocutaneous Lymph Node Syndrome/complications ; Mucocutaneous Lymph Node Syndrome/diagnosis ; Mucocutaneous Lymph Node Syndrome/genetics ; Mutation ; Plasma Cells
    Chemical Substances Antibodies ; Biomarkers
    Language English
    Publishing date 2022-03-15
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 424427-8
    ISSN 1872-9142 ; 0161-5890
    ISSN (online) 1872-9142
    ISSN 0161-5890
    DOI 10.1016/j.molimm.2022.03.011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Detection of Hepatitis B Virus-Host Junction Sequences in Urine of Infected Patients.

    Lin, Selena Y / Su, Yih-Ping / Trauger, Evan R / Song, Benjamin P / Thompson, Emilie G C / Hoffman, Malcolm C / Chang, Ting-Tsung / Lin, Yih-Jyh / Kao, Yu-Lan / Cui, Yixiao / Hann, Hie-Won / Park, Grace / Shieh, Fwu-Shan / Song, Wei / Su, Ying-Hsiu

    Hepatology communications

    2021  Volume 5, Issue 10, Page(s) 1649–1659

    Abstract: Integrated hepatitis B virus (HBV) DNA, found in more than 85% of HBV-associated ...

    Abstract Integrated hepatitis B virus (HBV) DNA, found in more than 85% of HBV-associated hepatocellular carcinomas (HBV-HCCs), can play a significant role in HBV-related liver disease progression. HBV-host junction sequences (HBV-JSs), created through integration events, have been used to determine HBV-HCC clonality. Here, we investigate the feasibility of analyzing HBV integration in a noninvasive urine liquid biopsy. Using an HBV-targeted next-generation sequencing (NGS) assay, we first identified HBV-JSs in eight HBV-HCC tissues and designed short-amplicon junction-specific polymerase chain reaction assays to detect HBV-JSs in matched urine. We detected and validated tissue-derived junctions in five of eight matched urine samples. Next, we screened 32 urine samples collected from 25 patients infected with HBV (5 with hepatitis, 10 with cirrhosis, 4 with HCC, and 6 post-HCC). Encouragingly, all 32 urine samples contained HBV-JSs detectable by HBV-targeted NGS. Of the 712 total HBV-JSs detected in urine, 351 were in gene-coding regions, 11 of which, including TERT (telomerase reverse transcriptase), had previously been reported as recurrent integration sites in HCC tissue and were found only in the urine patients with cirrhosis or HCC. The integration breakpoints of HBV DNA detected in urine were found predominantly (~70%) at a previously identified integration hotspot, HBV DR1-2 (down-regulator of transcription 1-2). Conclusion: HBV viral-host junction DNA can be detected in urine of patients infected with HBV. This study demonstrates the potential for a noninvasive urine liquid biopsy of integrated HBV DNA to monitor patients infected with HBV for HBV-associated liver diseases and the efficacy of antiviral therapy.
    MeSH term(s) Adult ; Aged ; Attachment Sites, Microbiological/genetics ; Carcinoma, Hepatocellular/genetics ; Carcinoma, Hepatocellular/urine ; Carcinoma, Hepatocellular/virology ; DNA, Viral/genetics ; DNA, Viral/urine ; Female ; Hepatitis B virus/genetics ; High-Throughput Nucleotide Sequencing ; Humans ; Liver Neoplasms/genetics ; Liver Neoplasms/urine ; Liver Neoplasms/virology ; Male ; Middle Aged ; Polymerase Chain Reaction ; Virus Integration/genetics
    Chemical Substances DNA, Viral
    Language English
    Publishing date 2021-08-25
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ISSN 2471-254X
    ISSN (online) 2471-254X
    DOI 10.1002/hep4.1783
    Database MEDical Literature Analysis and Retrieval System OnLINE

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