<abstract xmlns="http://www.w3.org/1999/xhtml"><p>There are no published data on the detection of tube agglutination (TA) 37°C-onJy antibodies by solid-phase (SP) red celi adherence assays using anti-IgG-coated indicator red cells. Thirteen examples of TA 37°C-only antibodies were tested by conventional SP methods. Four TA 37°C-only antibodies failed to react by SP. Three were anti-Le<sup>a</sup> considered clinically insignificant, and one was anti-E, an antibody of potential clinical significance. The remaining nine TA 37°C-only antibodies reacted by SP, including three anti-c, two anti-D, two anti-E, one anti-N. and one anti-M. The anti-M reacted with indicator red cells that lacked the red cell antigen and failed to react with IgG-coated indicator red cells whose anti-IgG component had been neutralized, indicating the antibody contained an IgG component. Two anti-D and one anti-c continued to react in an SP test using neutralized anti-IgG antigen-positive indicator red cells, i.e., indicator binding independent of antiglobulin, suggesting an IgM nature to these antibodies. Therefore, many TA 37°C-oniy antibodies can be detected by SP either through detection of an IgG component by the anti-IgG of the indicator red cells, or through IgM crosslinking of antigen-positive indicator red cells to antigen-positive SP reagent red cell membranes. <bold><italic>Immunobematology</italic></bold> 1996;12:27-29.</p></abstract>

There are no published data on the detection of tube agglutination (TA) 37°C-onJy antibodies by solid-phase (SP) red celi adherence assays using anti-IgG-coated indicator red cells. Thirteen examples of TA 37°C-only antibodies were tested by conventional SP methods. Four TA 37°C-only antibodies failed to react by SP. Three were anti-Lea considered clinically insignificant, and one was anti-E, an antibody of potential clinical significance. The remaining nine TA 37°C-only antibodies reacted by SP, including three anti-c, two anti-D, two anti-E, one anti-N. and one anti-M. The anti-M reacted with indicator red cells that lacked the red cell antigen and failed to react with IgG-coated indicator red cells whose anti-IgG component had been neutralized, indicating the antibody contained an IgG component. Two anti-D and one anti-c continued to react in an SP test using neutralized anti-IgG antigen-positive indicator red cells, i.e., indicator binding independent of antiglobulin, suggesting an IgM nature to these antibodies. Therefore, many TA 37°C-oniy antibodies can be detected by SP either through detection of an IgG component by the anti-IgG of the indicator red cells, or through IgM crosslinking of antigen-positive indicator red cells to antigen-positive SP reagent red cell membranes. Immunobematology 1996;12:27-29.

Detection of tube agglutination 37°C-onIy antibodies by solid-phase red cell adherence

Immunohematology

There are no published data on the detection of tube agglutination (TA) 37°C-onJy antibodies by solid-phase (SP) red celi adherence assays using...

Detection of tube agglutination 37°C-onIy antibodies by solid-phase red cell adherence

Data publikacji: 10 lis 2020

Zakres stron: 27 - 29

DOI: https://doi.org/10.21307/immunohematology-2019-742

© 1996 S. Rolih et al., published by Sciendo