American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons·2013
Human immune complexes (IC) bind to monocytes and neutrophils. Factors like low pH and trypsin affect this binding, influencing immune cell interactions and potential therapeutic targets.
Area of Science:
Immunology
Cell Biology
Background:
Soluble human serum albumin anti-albumin immune complexes (IC) are involved in immune responses.
Monocytes and polymorphonuclear leucocytes (PMN) are key immune cells that interact with ICs.
Purpose of the Study:
To investigate the binding characteristics of anti-albumin ICs to human monocytes and PMN.
To explore factors influencing IC binding, including pH and enzymatic treatment.
Main Methods:
In vitro binding assays using freshly isolated human peripheral blood monocytes and PMN.
Saturation binding studies and inhibition assays with aggregated IgG subclasses.
Incubation at low pH (6.0) and treatment with trypsin.
Main Results:
Both monocytes and PMN exhibit saturable binding of ICs, with PMN having more binding sites.
Low pH (6.0) enhances IC binding through increased affinity in PMN and increased site number in monocytes.
Trypsin treatment differentially affects binding: suspension treatment increases sites and affinity, while adherent treatment primarily increases monocyte affinity.
Conclusions:
Human monocytes and PMN possess specific binding sites for anti-albumin ICs.
Environmental factors like pH and cell surface modifications (trypsin) modulate IC binding affinity and site availability, impacting immune cell function.