Expression of CD21 and CD23 during Human Fetal Development

Thornton, Catherine A.

doi:10.1203/01.pdr.0000023172.89966.50

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Cited by 3 publications

(1 citation statement)

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“…CD23 is a low‐affinity Fcε receptor expressed on B lymphocytes with variable intensity 9,10 . It was first described as a low‐affinity IgE receptor, a surface marker on Epstein–Barr virus‐transformed B cells and as an activation antigen on B cells 11–13 .…”

Section: Discussionmentioning

confidence: 99%

Significant high expression of CD23 in follicular lymphoma of the inguinal region

et al. 2007

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Section: Discussionmentioning

confidence: 99%

Significant high expression of CD23 in follicular lymphoma of the inguinal region

et al. 2007

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Coordination of Adaptive Immune Responses by C3

Erdei

Molnár

Csomor

et al.

The Complement System

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Abstract:Once triggered, complement activation leads to the generation of various C3 degradation products. Receptors for these fragments are expressed by cells of both the innate and adaptive immune system, enabling complement activation to exert both indirect and direct effects on adaptive immune responses. The anaphylatoxin C3a recruits and primes granulocytes and macrophages and influence lymphocyte functions as well. C3 cleavage fragments covalently linked to the antigen influence its fate on the level of the organism and on the level of the cell as well. C3 receptors present on lymphocytes set the threshold for cellular activation and may thereby also shape the immune repertoire.

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Vaccination in the context of immunological immaturity

Arvin

Lewis

2005

The Grand Challenge for the Future

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Expression of CD21 and CD23 during Human Fetal Development

Cited by 3 publications

References 12 publications

Significant high expression of CD23 in follicular lymphoma of the inguinal region

Significant high expression of CD23 in follicular lymphoma of the inguinal region

Coordination of Adaptive Immune Responses by C3

Vaccination in the context of immunological immaturity

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