Sentence examples for migration to peripheral from inspiring English sources
Although their exact lifespan is debated, it is of general consensus that neutrophils leave the BM with a default pro-apoptotic program that can be inhibited by stimuli received upon migration to peripheral tissues [18, 19].
Memory CD8 T cells have an enhanced capacity to control secondary antigen exposure, through more efficient proliferation, rapid acquisition of effector functions, IFN-γ and TNF-α production, and migration to peripheral sites of infection [41].
These transfected DCs are activated by the pressure from bombardment and undergo migration to peripheral lymphoid organs.
The expression of CD62L, which is important for T-cell migration to peripheral tissues, was also normal.
Such continual but transient migration to peripheral sites may represent an adaptation that facilitates uptake by haematophagous triatomine vectors.
TN are CD45RA+ and express CCR7 for peripheral lymph node homing but lack receptors such as CCR4 and CCR6 for the migration to peripheral tissues [ 2, 16- 18].
Regulatory T cells (CD4+CD25+Foxp3+) are known to be involved in suppressing immune responses [ 61], and they also express CCR5 on their surface, enhancing migration to the peripheral inflamed tissues [ 62, 63] and gravid uterus [ 64] through interaction with CCR5 ligands.
The observation that abnormal B-cell development in KO mice prompted us to evaluate the expression pattern of a multitude of different transcriptional factors by real-time PCR, which have been linked to distinct stages of the life of B lymphocytes, such as differentiation in the BM, migration to the peripheral organs and antigen-induced activation.
T cells show a bias in their migration pathways: some migrate preferentially to peripheral lymph nodes, some to mucosal tissues and some to peripheral tissues such as skin.
In addition, stem cells can be "mobilized" in response to hematopoietic stress, rapidly undergoing expansion and migration to repopulate the peripheral hematopoietic compartments.
The kinetics of engraftment reflects the human disease, leading to bone marrow (BM) infiltration, followed by migration to the spleen, peripheral blood and other haematopoietic organs [ 2- 4].
