Thanks!! I looked at the article and am not sure it applies. We treat our antibodies of undetermined specificity as clinically significant and will always provide AHG crosmatched blood even if the antibody is not showing (for our sickles we would honor their full phenotype). But in the case of an identified clinically insignificant (M, Lea, etc) we would not honor the full phenotype and I'm curious if there is any clinical evidence that confirms that. Since the point of honoring the phenotype of a patient with a clinically significant antibody is that they're a responder and now that they've formed one you don't want them to form any more, why would the formation of any antibody (significant or not) not indicate the patient is a responder. My thought is that the immune system doesn't know we label certain antibodies as clinically significant, so what's the difference? Thanks!