Sentence examples for subset recruitment from inspiring English sources

According to the observed peaks of the MIF proteins during cardiac surgery and the known kinetics of leukocyte subset recruitment into the injured heart, peripheral blood monocytes (PBMCs), representing mid-acutely recruited inflammatory cells, were used to study the contribution of MIF proteins.

However, in vivo, the precise subset of DCs responsible for inducing pathogenic versus protective T cell responses, the pattern of DC-derived cytokines that drive these T cell responses, and the extent to which DC subset recruitment and cytokine production are regulated by the pulmonary environment and genetics in asthma-susceptible and resistant hosts, remains unclear.

Impaired monocyte subset recruitment in CCR2-/ and CCR2-/-CCR6-/ mice resulted in reduced HSC activation and diminished liver fibrosis.

Therefore, in the present study, we propose to decipher in vivo in real time the kinetic of macrophage subset recruitment, their behaviour and their phenotypic plasticity at the molecular level during a multiple-step inflammatory process.

The recently identified cellular and molecular pathways for monocyte subset recruitment, macrophage differentiation and interactions with other hepatic cell types in injured liver may therefore represent interesting novel targets for future therapeutic approaches in liver fibrosis.

The modulation of monocyte-subset recruitment into the liver via chemokines/chemokine receptors and their subsequent differentiation may therefore indeed represent promising approaches for therapeutic interventions in human liver fibrosis [ 51].

Panel (B) splits the data in two subsets: the first subset considers recruitment activity before 15-M, the day of the first mass demonstrations; the second subset tracks activity after 15-M.

It has been indicated that several chemokine receptors including CCR1, CCR2, CCR3, CCR5, CCR6, CCR7, CCR9, CCR10, CXCR3, CXCR4, CXCR5, and ChemR23 are involved in control of different subsets of DCs recruitment to periphery tissues and migration to secondary lymphoid tissues or migration within lymphoid tissues.

Recruitment in the ER negative subset was stopped prematurely after recruitment of 12 patients because of lack of response and rapid progression in these patients.

Subjects in this study are a subset of subjects whose recruitment has been described in detail elsewhere [ 25].

Thus, a permanent decrease of circulating CD27 IgD IgM B cells could be the result of self-antigen activation of auto-reactive B cells contained in elevated proportions in this subset, and their subsequent recruitment into lymphoid tissues.