Adam Dingens, PhD, MS
@adamdingens
Viral functional genomics, immune escape, tech dev & vaccines
ID: 2479194139
06-05-2014 03:26:46
40 Tweet
289 Followers
587 Following
I've long advocated the use of DMS-approaches to understand escape from monoclonal and pooled antibodies during their development as antiviral therapeutics, as well as during viral surveillance to guide their clinical use. Here's a great example why! science.sciencemag.org/content/early/…
Half a million Americans have died of COVID-19. I wrote for The New Yorker about what this terrible milestone tells us, and what we still have to learn. newyorker.com/science/elemen…
We have completely mapped #SARS_CoV_2 mutations that escape binding by LY-CoV555 (antibody that forms the basis for Eli Lilly's bamlanivimab) both alone & in cocktail with LY-CoV016 in a new study led by Tyler Starr w/ Allie Greaney & Adam Dingens, PhD, MS: biorxiv.org/content/10.110… (1/n)
We've created an interactive website to visualize >100,000 experimental measurements of how mutations to #SARSCoV2 RBD affect binding by antibodies & sera: jbloomlab.github.io/SARS2_RBD_Ab_e… Explore it to examine a wealth of information about the antigenic effects of viral mutations. (1/n)
Awesome to see more high-throughput antibody escape tech come on board, particularly from industry - where resulting data can more quickly be used to evaluate, engineer, and pool mAbs under clinical development. Great job A-Alpha Bio !
I passed my thesis defense yesterday, “Understanding #SARSCoV2 antigenic drift using complete genotype-to-phenotype maps.” It has been an absolute privilege to be a graduate student in the Bloom Lab at the Fred Hutch Cancer Center and University of Washington - MSTP.