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May 24, 2005European Journal of ImmunologyOpen Access

Both the pre-BCR and the IL-7Rα are essential for expansion at the pre-BII cell stagein vivo

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Key result

Combined IL-7Rα and pre-BCR deficiency in mice severely depletes pre-BII and peripheral B cells.

Why the study?

The in vivo relationship between the pre-BCR and the IL-7Ralpha in pre-BII cell expansion had not been previously examined.

Population

Mice lacking both pre-BCR and IL-7Ralpha receptors

Comparison

Mice lacking both receptors vs mice lacking only pre-BCR or only IL-7Ralpha

Design

Preclinical genetic deletion study

Authors

LELena ErlandssonLund UniversitySLSteve LicenceBabraham InstituteFGFabrina GaspalUniversity College Birmingham

Discussion

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Implication

Supports dual receptor requirement for murine pre-BII expansion; leaves open human translational relevance.

Structured PICO

P
Population
Mice lacking both pre-BCR and IL-7Ralpha receptors
E
Exposure
Genetic deletion of both pre-BCR and IL-7Ralpha
C
Comparator
Mice lacking only pre-BCR or only IL-7Ralpha
O
Outcome
Pre-BII cell population expansionsurrogate

Both IL-7Ralpha and pre-BCR are required for optimal pre-BII cell expansion in vivo, and pre-BCR does not mediate IL-7Ralpha down-regulation.

Cite This Study

Erlandsson et al. (2005) studied B cell development. Deficiency in both pre-BCR and IL-7Rα vs. Wild-type or single receptor deficiency was evaluated on pre-BII cell population expansion. Deficiency in both IL-7Rα and pre-BCR receptors in mice results in a severe reduction of the pre-BII cell population and depletion of the peripheral B cell pool.

synapsesocial.com/papers/6aa957d511a60bccbd26513ehttps://doi.org/10.1002/eji.200425821
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