T
Takuya Tada
Researcher at New York University
Publications - 51
Citations - 1242
Takuya Tada is an academic researcher from New York University. The author has contributed to research in topics: Antibody & Medicine. The author has an hindex of 14, co-authored 33 publications receiving 545 citations. Previous affiliations of Takuya Tada include University of Tokyo & National Institutes of Health.
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Journal ArticleDOI
MARCH8 inhibits HIV-1 infection by reducing virion incorporation of envelope glycoproteins.
Takuya Tada,Yanzhao Zhang,Yanzhao Zhang,Takayoshi Koyama,Minoru Tobiume,Yasuko Tsunetsugu-Yokota,Shoji Yamaoka,Hideaki Fujita,Kenzo Tokunaga +8 more
TL;DR: The findings indicate that MARCH8 is highly expressed in terminally differentiated myeloid cells, and that it is a potent antiviral protein that targets viral envelope glycoproteins and reduces their incorporation into virions.
Posted ContentDOI
Neutralization of viruses with European, South African, and United States SARS-CoV-2 variant spike proteins by convalescent sera and BNT162b2 mRNA vaccine-elicited antibodies
Takuya Tada,Belinda M Dcosta,Marie I. Samanovic-Golden,Ramin S. Herati,Amber Cornelius,Mark J. Mulligan,Nathaniel R. Landau +6 more
TL;DR: Findings suggest that antibodies elicited by primary infection and by the BNT162b2 mRNA vaccine are likely to maintain protective efficacy against SARS-CoV-2 variants but that the partial resistance of virus with the B.1.1-1.351 spike protein could render some individuals less well protected, supporting a rationale for the development of modified vaccines containing E484K.
Posted ContentDOI
Comparison of Neutralizing Antibody Titers Elicited by mRNA and Adenoviral Vector Vaccine against SARS-CoV-2 Variants
Takuya Tada,Hao Zhou,Marie I. Samanovic,Belinda M Dcosta,Amber Cornelius,Mark J. Mulligan,Nathaniel R. Landau +6 more
TL;DR: In this paper, neutralizing antibody titers elicited by mRNA-based and an adenoviral vector-based vaccine against variant pseudotyped viruses were compared, showing that BNT162b2 and mRNA-1273-elicited antibodies showed modest neutralization resistance against Beta, Delta, Delta plus and Lambda variants.
Journal ArticleDOI
An ACE2 Microbody Containing a Single Immunoglobulin Fc Domain Is a Potent Inhibitor of SARS-CoV-2.
Takuya Tada,Chen Fan,Jennifer S. Chen,Ramanjit Kaur,Kenneth A. Stapleford,Harry B. Gristick,Belinda M Dcosta,Craig B. Wilen,Crina M. Nimigean,Nathaniel R. Landau +9 more
TL;DR: An improved soluble ACE2 is reported, termed a “microbody” in which the ACE2 ectodomain is fused to Fc domain 3 of the immunoglobulin heavy chain and it inhibits entry of β coronaviruses and virus with the variant D614G spike.
Posted ContentDOI
Decreased neutralization of SARS-CoV-2 global variants by therapeutic anti-spike protein monoclonal antibodies
TL;DR: In this paper, the authors tested monoclonal antibodies REGN10933 and REGN10987 that are used in combination, for their ability to neutralize SARS-CoV-2 variants B.1.7, mink cluster 5 and COH.