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Published on: April 2, 2014
Development of Host Immune Response to Bacteriophage in a Lung Transplant Recipient on Adjunctive Phage Therapy for a
Jennifer M Dan1,2, Susan M Lehman3, Rita Al-Kolla1
1Center for Infectious Diseases and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California, USA.
Abstract:
Bacteriophage therapy is the use of viruses to kill bacteria for the treatment of antibiotic-resistant infections. Little is known about the human immune response following phage therapy. We report the development of phage-specific CD4 T cells alongside rising phage-specific immunoglobulin G and neutralizing antibodies in response to adjunctive bacteriophage therapy used to treat a multidrug-resistant Pseudomonas aeruginosa pneumonia in a lung transplant recipient. Clinically, treatment was considered a success despite the development phage-specific immune responses.
Insights
Bacteriophage therapy uses viruses to combat antibiotic-resistant bacteria. This study observed immune responses, including T cells and antibodies, during successful phage treatment for Pseudomonas aeruginosa pneumonia.
Area of Science:
- Immunology
- Microbiology
- Infectious Diseases
Background:
- Bacteriophage therapy is a promising alternative for treating antibiotic-resistant bacterial infections.
- The human immune response to bacteriophage therapy remains largely uncharacterized.
- Pseudomonas aeruginosa is a common cause of difficult-to-treat lung infections, particularly in immunocompromised individuals.
Purpose of the Study:
- To investigate the human immune response during adjunctive bacteriophage therapy.
- To characterize the development of phage-specific immune markers in a clinical setting.
- To assess the safety and efficacy of bacteriophage therapy in a lung transplant recipient.
Main Methods:
- Case report of a lung transplant recipient with multidrug-resistant Pseudomonas aeruginosa pneumonia.
- Administration of adjunctive bacteriophage therapy.
- Monitoring of phage-specific CD4 T cell responses.
- Measurement of phage-specific immunoglobulin G (IgG) and neutralizing antibodies.
Main Results:
- Successful clinical treatment of multidrug-resistant Pseudomonas aeruginosa pneumonia.
- Development of detectable phage-specific CD4 T cell responses.
- Rising levels of phage-specific IgG and neutralizing antibodies were observed.
- Phage-specific immune responses did not preclude successful clinical outcome.
Conclusions:
- Adjunctive bacteriophage therapy can elicit robust, specific immune responses in humans.
- The development of phage-specific immunity does not necessarily contraindicate successful therapeutic outcomes.
- Further research is warranted to fully understand the immunomodulatory effects of bacteriophage therapy.
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