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Minipool technology to prepare immunoglobulins to treat primary immunodeficiency and fight viral infections, such as Ebola, in developing countries

A study publishing in describes a new, pragmatic, method for the production of immunoglobulin G (IgG) from human plasma in . IgG are therapeutic preparations on the WHO Medicine Essential List that are used to treat patients with primary immune immunodeficiency (PID) and to fight various infectious diseases. PID affects approximately 1 out of 5000 individuals. IgG are manufactured mostly in sophisticated facilities located in advanced economies and are produced from plasma collected in the USA or Europe. There are serious shortages of IgG worldwide, leaving PID patients in the developing world without treatment and therefore exposed to local viral and bacterial pathogens.

This simple methodology reported in PLOS Neglected Tropical Diseases allows the preparation of virally-inactivated IgG from small pool of plasma using disposable equipment and medical devices. It can be implemented to fractionate plasma from developing countries without the need to build a pharmaceutical facility. IgG made from local plasma have the ideal mix of antibodies suited to fight local viral and bacterial pathogens. The method could be ideal to prepare IgG from convalescent plasma, as is the case following the Ebola epidemics in West African countries.

Thierry Burnouf, corresponding author of the study and closely involved in the development of the procedure, also Director of the Graduate Institute of Biomedical Materials and Tissue Engineering at Taipei Medical University (Taiwan), indicates that “making a simple, efficient, and cost-effective can often be more difficult than making it sophisticated. This minipool is a robust and pragmatic way to prepare IgG with good safety and purity levels; although initially targeting the treatment of PID, the can also be of value for preparing anti-Ebola virus IgG, or other IgG against emerging pathogens, using a minipool of 20 convalescent plasma donations.”

“We have developed and implemented this technology with great success in our production center which is also preparing virally inactivated plasma and cryoprecipitate to treat patients with various bleeding disorders. The clinical studies performed in PID children are showing the safety and efficacy of the minipool IgG product to restore normal IgG levels and decrease the incidence of infections” said Magdy El-Ekiaby, first author of the study, Director of the Shabrawishi Hospital Blood Bank, and Egyptian Company for Biological Sciences in Cairo (Egypt), who has played a leading role in developing and implementing such minipool processes.

The authors note that the process could be implemented readily in blood establishments or national service centers after appropriate operator training and basic equipment acquisition. Critical parts of the process are performed in a closed-bag system and easy-to-use disposable equipment, do not present cleaning-related cross-contamination risks, and is affordable. It is far more feasible than current fractionation technologies for rapid implementation in low or medium income countries, therefore representing a pragmatic approach to address IgG shortages and to prepare convalescent IgG for passive immunotherapy against emerging infections.

Source

Minipool Caprylic Acid Fractionation of Plasma Using Disposable Equipment: A Practical Method to Enhance Immunoglobulin Supply in Developing Countries, Magdy El-Ekiaby, Mariángela Vargas, Makram Sayed, George Gorgy, Hadi Goubran, Mirjana Radosevic, Thierry Burnouf, PLOS Neglected Tropical Diseases, DOI:10.1371/journal.pntd.0003501, published 26 February 2015.

The study was supported by Shabrawishi Hospital. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Mirjana Radosevich is a member of Human Protein Process Sciences, a company which contributed scientifically to the development of the described method but has no financial interest. This does not alter our adherence to all PLOS NTDs policies on sharing data and materials.