ApoVax (United States)

El objetivo general de este estudio ha sido evaluar, la seguridad sistémica que sobre la presión arterial y la frecuencia cardíaca, tiene la inyección intracameral de adrenalina al inicio de cirugía de cataratas para obtener midriasis, en pacientes normales y pacientes con patología cardiovascular y diferentes grados de riesgo anestésico.
\nSe ha realizado un estudio estadístico sobre 777 pacientes intervenidos de cataratas. Dos grupos: a uno de los grupos se le aplicaron midriáticos tópicos: ciclopléjico, tropicamida y fenilefrina, y al otro los mismos midriáticos tópicos más adrenalina intracameral al 1/2.000
\nEl estudio estadístico comparativo de las medias de los parámetros investigados, no mostró diferencias estadísticamente significativas entre los grupos.
\nCONCLUSIÓN: la inyección intracameral de adrenalina al inicio de la cirugía de cataratas, no incrementa el riesgo sobre los parámetros estudiados en ninguno de los grupos, independientemente de si presentan o no patología cardiovascular o diferentes grados de riesgo anestésico.

Therapeutic subunit vaccines based on tumor-associated antigens (TAA) represent an attractive approach for the treatment of cancer. However, poor immunogenicity of TAAs requires potent adjuvants for therapeutic efficacy. We recently proposed the tumor necrosis factor family costimulatory ligands as potential adjuvants for therapeutic vaccines and, hence, generated a soluble form of 4-1BBL chimeric with streptavidin (SA-4-1BBL) that has pleiotropic effects on cells of innate, adaptive, and regulatory immunity. We herein tested whether these effects can translate into effective cancer immunotherapy when SA-4-1BBL was also used as a vehicle to deliver TAAs in vivo to dendritic cells (DCs) constitutively expressing the 4-1BB receptor. SA-4-1BBL was internalized by DCs upon receptor binding and immunization with biotinylated antigens conjugated to SA-4-1BBL resulted in increased antigen uptake and cross-presentation by DCs, leading to the generation of effective T-cell immune responses. Conjugate vaccines containing human papillomavirus 16 E7 oncoprotein or survivin as a self-TAA had potent therapeutic efficacy against TC-1 cervical and 3LL lung carcinoma tumors, respectively. Therapeutic efficacy of the vaccines was associated with increased CD4(+) T and CD8(+) T-cell effector and memory responses and higher intratumoral CD8(+) T effector/CD4(+)CD25(+)Foxp3(+) T regulatory cell ratio. Thus, potent pleiotropic immune functions of SA-4-1BBL combined with its ability to serve as a vehicle to increase the delivery of antigens to DCs in vivo endow this molecule with the potential to serve as an effective immunomodulatory component of therapeutic vaccines against cancer and chronic infections.