“
“Sustained research efforts over the last 50 years have revealed

a considerable amount of information about immunity to taeniid cestode infections in the parasites’ intermediate hosts. As a product of this research, a series of effective recombinant vaccines have been developed which have no parallel in any other group of parasitic organisms. There are, however, many important aspects relating to immunity that remain to be elucidated. Some concepts have come to be firmly held as Pexidartinib solubility dmso facts and yet the supportive data are either conflicting or unconfirmed. This review considers the phenomenon of immunity to re-infection with taeniid cestodes in their intermediate hosts, examining carefully the nature of the evidence that is available to support conclusions that have been drawn in this area. “
“Replacement therapy with exogenous factor VIII (FVIII) to treat haemorrhages or used in prophylaxis induces inhibitory anti-FVIII immunoglobulin G (IgG) in some patients with haemophilia A. Therapeutic strategies to prevent

the onset of the deleterious anti-FVIII immune response are still lacking. Maternal IgG is transferred to the offspring during fetal and neonatal life. While protecting the offspring from bacterial and viral infections, maternal IgG may alter the repertoires of T and B lymphocytes, and may impair vaccination in early infancy. Using CHIR-99021 cell line haemophilic mice, we demonstrate that the transfer of maternal anti-FVIII IgG modulates the onset of anti-FVIII inhibitory IgG in early adulthood. The protective effect is reproduced upon reconstitution of naive mice with anti-FVIII IgG, see more suggesting that the reduced ability to mount an anti-FVIII immune response is the result of an interference between circulating anti-FVIII IgG and the administered FVIII rather than to a profound remodelling of lymphocyte repertoires occurring during the ontogeny of the immune system. Administration of exogenous factor VIII (FVIII) to patients with haemophilia A leads, in up to 30%

of the cases, to the development of neutralizing anti-FVIII alloantibodies that inhibit the pro-coagulant activity of FVIII. Different therapeutic strategies are being used to eliminate FVIII inhibitors, such as the administration of B-cell-depleting anti-CD20 antibodies (Rituximab®, Genentech Inc, South San Francisco, CA, USA) or the induction of immune tolerance upon repeated injection of high doses of FVIII.1 In patients, prophylaxis has been proposed as one of the rare solutions towards a reduction of the risk for the onset of the deleterious anti-FVIII immune response.2,3 During fetal life, maternal immunoglobulin G (IgG) of the IgG1 subclass is delivered through the placenta to the fetus via interactions with the neonatal Fc receptor (FcRn).