Thanks for that link.   CD4 is expressed on helper T cells and it promotes 
adhesion to antigen-presenting cells.
CD8 is the same but for cytotoxic T cells and different kinds of antigens.   
CD3 accessory proteins help signal from either of those into helper and 
cytotoxic cells that something has gone wrong.  The helper T cells will help 
activate an antibody response from B cells and their cytotoxic siblings, and 
the cytotoxic cells kill off infected cells.   I don't know how values across 
the board would lead to a cytokine storm -- it sounds like immunodeficiency.  

On 4/23/20, 2:04 PM, "Friam on behalf of uǝlƃ ☣" <[email protected] on 
behalf of [email protected]> wrote:

    Suppressed T cell-mediated immunity in patients with COVID-19: A clinical 
retrospective study in Wuhan, China
    https://www.journalofinfection.com/article/S0163-4453(20)30223-1/abstract
    
    Does anyone here have a sense for the types of conditions (cf covid19 
comorbidities) that cluster around all 3 proteins? My naive googling returns 
comments about graft-vs-host and various autoimmune conditions and 
immunosuppressive therapies. But I'm having trouble getting a feel for how they 
might all cluster together. Maybe it's simply that lower amounts of *any* of 
the 3 subsets produces a higher risk for those with covid19? But I keep hearing 
that the "cytokine storm" is more than just an effect, it may loop back and be 
part of the problem.
    
    -- 
    ☣ uǝlƃ
    
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