We determined CR1, CD35 the C3b, C4b receptor density, C3b/C3bi and C4d deposits densities on Erythrocytes (E) in 51 COVID-19 patients undergoing O2 therapy or assisted ventilation in ICU units in Rheims France. A clear acquired decrease of CR1 density of E from COVID-19 patients was observed, particularly among fatal cases, and paralleling several severity parameters.
Deposits of C4d largely above values observed in normal individuals, mostly without C3 deposits, have been observed in more than 80% of the patients, reminiscent of the sub endothelial pericapil-lary deposits in organ transplant rejection, already observed on E in parallel, as well as also observed on E in clinical SLE flares.
Conversely, significant C3 deposits were only observed among 1/4 of the patients. The decrease of CR1/E density, and the detection of virus spike, C3 or C4 fragment on E, among COVID-19 pa-tients, are likely to be two aspects of the same phenomenon of immune complexes or complement fragment coated cell debris handling and clearance.
Measurement of C4d deposit on E might represent a way for assessing inflammation and comple-ment activation occurring in organ capillaries. CR1/E decrease might represent a cumulative index of complement activation in COVID-19 patients.
Taken together, these original findings stress on the participation of the complement regulatory pro-teins in that disease and evidence that E matter in immune mechanisms in COVID-19 patients.
The use of CR1, or CR1-like molecules with the aim of down regulating complement activation and inflammation for therapy should also be considered.