Abstract

In the eighth decade of the last century extensive clinical delayed-type hypersensitivity (DTH) skin tests to an intradermal injection of a pharmaceutical allogeneic human Placenta Suspension (phPS) performed in obstetrical, gynecological and control group patients have shown positive reaction in 239 patients with clinical conditions having been as histopatrhological substratum, a hypoxia-induced adaptive/reactive epithelial cell proliferation, e.g. syncytiotrophoblastic cell hyperplasia, endometrial cell hyperplasia, or different gynecological cancers. Because the immune response against phPS has shown antigenc similarities between normal placental and endometrial hyperplastic cells and different kinds of cancer cells and because many cancers adopt an embryonic stem-like gene expression pattern, it is suggested that the profile of hypoxia-promoting placental and endometrial stem cell proliferation is more embryonic-like, and that the immune respose against phPS is expected to cross-react with tumor cells in vivo. In the process of persistent growth and accelerated oxygen consumption by hyperplastic cytotrophoblastic cells and neoplastic cells in a hypoxic microenvironment, a basic shift in energy metabolism is accompanied by appearance of heat shock proteins (HSPs), of fetal isoenzymes and of membrane glycoproteins (reappearance of oncofetal antigens, OFAs), which, as result of their overexpression/amplification may induce a host immunological response. Thus, it is assumed that phPS prepared from full-term human placentas delivered after a spontaneous labor comprises stem/progenitor cells reverted to a proliferative embryonic stem cell-like-state upon exposure to labor-inducing intrmittent placental hypoxia and that by expressing HSP/OFAs could immunize to generate immune response againjst a variety of antigens that are shared by different kinds of epithelial cancers. This immunological feature of phPS qualifies is as a vaccine-related product that may be used for a preventive cancer vaccine when mixed with a potent adjuvant (BCG-Vaccine) and given normal healthy individuals.

Highlights

  • IntroductionA retrospective analysis of our previous studies [1] and our proposed pharmaceutical allogeneic human Placenta-Lysates/BCG-vaccine strategy design for cancer prevention [2], based on the assumption that placenta shares identical growth mechanisms, antigenic determinants, and immune-escape properties with cancer cells, combined with present knowledges may provide additional insight in this vaccination approach

  • The field of tumor immunology has made great advancements in recent years

  • According to the clinical and histopathlogical diagnosis, two large groups have resulted in which obstetrical and gynecological patients with different clinical conditions have shown positive cutaneous delayed-type hypersensitivity (DTH)-response to pharmaceutical allogeneic human Placenta Suspension (phPS): a group of benign obstetrical and gynecological clinical conditions having as histopathological substratum adaptive syncytiotrophoblast-cell hyperplasia (98 pts.), or reactive/adaptive endometrial cell hyperplasia (76 pts.) and a group of different gynecological cancers (65 pts.)

Read more

Summary

Introduction

A retrospective analysis of our previous studies [1] and our proposed pharmaceutical allogeneic human Placenta-Lysates/BCG-vaccine strategy design for cancer prevention [2], based on the assumption that placenta shares identical growth mechanisms, antigenic determinants, and immune-escape properties with cancer cells, combined with present knowledges may provide additional insight in this vaccination approach. Proteins that are expressed by both malignant and healthy fetal tissues (the placental-fetal complex) are recognized as oncofetal antigens (OFA). These antigens are associated with cell proliferation and differentiation and are produced in high concentrations in pregnancy and malignancy [3]. Based on the assumption that developing placenta shares identical growth mechanisms, antigenic determinants, and immune-escape properties with cancer cells, immunological cross-reactivity between placental antigens and cancer antigens was investigated

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call