Full text

 

10.1186/s40409-018-0153-z 
 

Research article - Vol. 24, 2018

 

Quality of horse F(ab′)2 antitoxins and antirabies immunoglobulins: protein content and anticomplementary activity

 

Carla Cristina Squaiella-Baptistão1, Fábio Carlos Magnoli1, José Roberto Marcelino2, Osvaldo Augusto Sant’Anna1, Denise V. Tambourgi1 

 

1 Laboratório de Imunoquímica, Instituto Butantan, Av. Vital Brazil, 1500, São Paulo, SP CEP 05503-900, Brazil

2 Seção de Processamento de Plasmas Hiperimunes, Instituto Butantan, Av. Vital Brazil, 1500, São Paulo, SP CEP 05503-900, Brazil

 

ABSTRACT

Background

Among other applications, immunotherapy is used for the post-exposure treatment and/or prophylaxis of important infectious diseases, such as botulism, diphtheria, tetanus and rabies. The effectiveness of serum therapy is widely proven, but improvements on the immunoglobulin purification process and on the quality control are necessary to reduce the amount of protein aggregates. These may trigger adverse reactions in patients by activating the complement system and inducing the generation of anaphylatoxins. Herein, we used immunochemical methods to predict the quality of horse F(ab′)2 anti-botulinum AB, anti-diphtheric, antitetanic and anti-rabies immunoglobulins, in terms of amount of proteins and protein aggregates.

 

Methods

Samples were submitted to protein quantification, SDS-PAGE, Western blot analysis and molecular exclusion chromatography. The anticomplementary activity was determined in vitro by detecting the production of C5a/C5a desArg, the most potent anaphylatoxin. Data were analyzed by one-way ANOVA followed by Tukey's post-test, and differences were considered statistically significant when p < 0.05.

 

Results

Horse F(ab′)2 antitoxins and anti-rabies immunoglobulin preparations presented different amounts of protein. SDS-PAGE and Western blot analyses revealed the presence of protein aggregates, non-immunoglobulin contaminants and, unexpectedly, IgG whole molecules in the samples, indicating the non-complete digestion of immunoglobulins. The chromatographic profiles of antitoxins and anti-rabies immunoglobulins allowed to estimate the percentage of contaminants and aggregates in the samples. Although protein aggregates were present, the samples were not able to induce the generation of C5a/C5a desArg in vitro, indicating that they probably contain acceptable levels of aggregates.

 

Conclusions

Anti-botulinum AB (bivalent), anti-diphtheric, antitetanic and anti-rabies horse F(ab′)2 immunoglobulins probably contain acceptable levels of aggregates, although other improvements on the preparations must be carried out. Protein profile analysis and in vitro anticomplementary activity of F(ab′)2 immunoglobulin preparations should be included as quality control steps, to ensure acceptable levels of aggregates, contaminants and whole IgG molecules on final products, reducing the chances of adverse reactions in patients.

 

Keywords Heterologous immunoglobulin; F(ab′)2 fragment; Antitoxins; Anti-rabies; Protein profile; Complement system

 

Received: December 12, 2017.

Accepted: June 06, 2018.

 

Correspondence: carla.baptistao@butantan.gov.br

 

Author's contributions

CCSB performed the experiments, analyzed the data, discussed the results and wrote the manuscript. FCM carried out the molecular exclusion chromatographic runs, discussed the results and wrote the respective methods section. JRM provided the samples and discussed the results. OAS discussed the results and wrote the manuscript. DVT conceived the project, discussed the results and wrote the manuscript. All authors read and approved the final manuscript.

 

Competing interests

The authors declare that they have no competing interests.