1981Infection and ImmunityOpen access

Restoration by Normal Human Immunoglobulin G of Deficient Serum Opsonization for Streptococcus pneumoniae in Sickle Cell Disease

Ann B. Bjornson, Jeffrey S. Lobel, Patricia I. Magnafichi, Beatrice C. Lampkin

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Abstract

Supplementation of sera from four children with sickle cell disease with untreated or heated normal human serum or with normal human immunoglobulin G restored opsonic activity for serotype 10 Streptococcus pneumoniae, whereas supplementation with normal human immunoglobulin M did not.

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What this paper is about

Supplementation of sera from four children with sickle cell disease with untreated or heated normal human serum or with normal human immunoglobulin G restored opsonic activity for serotype 10 Streptococcus pneumoniae, whereas supplementation with normal human immunoglobulin M did not.

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Available abstract

Supplementation of sera from four children with sickle cell disease with untreated or heated normal human serum or with normal human immunoglobulin G restored opsonic activity for serotype 10 Streptococcus pneumoniae, whereas supplementation with normal human immunoglobulin M did not.

Key concepts: Antibody opsonization, Streptococcus pneumoniae, Opsonin, Antibody, Biology, Immunoglobulin G, Serotype, Immunology

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Restoration by Normal Human Immunoglobulin G of Deficient Serum Opsonization for Streptococcus pneumoniae in Sickle Cell Disease — Research Paper | ScholarLens