Host-Pathogen Interactions and Monoclonal Antibody Therapeutics

A special issue of Pathogens (ISSN 2076-0817). This special issue belongs to the section "Vaccines and Therapeutic Developments".

Deadline for manuscript submissions: 15 August 2024 | Viewed by 3196

Special Issue Editors


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Guest Editor
Cleveland Clinic Florida Research and Innovation Center, Port St. Lucie, FL 34987, USA
Interests: monoclonal antibodies; vaccines; hepatitis C virus; influenza virus; immunotherapy
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
Microbiology and Virology Laboratory, Vita-Salute University, San Raffaele, 20132 Milan, Italy
Interests: monoclonal antibodies; vaccines; hepatitis C virus; influenza virus; immunotherapy
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Since the description of the first reliable methodology for developing monoclonal antibodies (mAbs) by Köhler and Milstein in 1975 using the hybridoma technique, tremendous advances in their generation, characterization, engineering and expression have been made.

The great potential of these molecules, both from a laboratory and medical perspective, was immediately evident to the two scientists above, who were awarded the Nobel prize in Physiology or Medicine in 1984 for their discovery. In their seminal Nature paper of 1975, the authors state that “the manufacture of predefined specific antibodies by means of permanent tissue culture cell lines is of general interest” and after having described their work, they conclude that “such cells [the hybridomas] can be grown in vitro in massive cultures to provide specific antibody” and “such cultures could be valuable for medical and industrial use”. 

The hybridoma methodology is still used today by several investigators, but new technologies have been developed and described, especially with the advent of next-generation sequencing, and have been massively deployed in the field of antibody discovery, especially in the last decade. These new technologies are mainly characterized by high-throughput and rapidity, with an overall turnaround time from mAb discovery to full characterization as short as one month. These new technologies have further increased the importance of mAbs even today, especially during the SARS-CoV-2 pandemic, where a plethora of SARS-CoV-2-specific mAbs have been reported in the literature as potential therapeutic tools.

Suggested topics for this Special Issue include, but are not limited to, new mAbs against infectious pathogens, the host immune response, the identification of potential viral antigens and epitopes, and new techniques for mAb discovery, development, production and engineering. There is no limitation on the type of contribution; original articles, communications, case reports, and reviews are all welcome. Your valuable input will enrich the current state of knowledge and contribute to the control of infectious diseases.

Dr. Giuseppe A. Sautto
Dr. Roberta Antonia Diotti
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Pathogens is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • monoclonal antibodies (mAbs)
  • next-generation sequencing
  • hybridoma
  • B cells
  • infectious diseases

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Published Papers (2 papers)

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19 pages, 3889 KiB  
Article
Isolation and Production of Human Monoclonal Antibody Proteins against a Toxocara canis Excretory–Secretory Recombinant Antigen
by Zamrina Baharudeen, Rahmah Noordin, Lim Theam Soon, Dinesh Balachandra, Nor Suhada Anuar, Fatin Hamimi Mustafa and Anizah Rahumatullah
Pathogens 2022, 11(11), 1232; https://doi.org/10.3390/pathogens11111232 - 25 Oct 2022
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Abstract
Toxocariasis is a widespread zoonotic parasitic disease with a significant socioeconomic impact, particularly on underprivileged communities. Limitations of existing diagnostic tools and vague presenting symptoms may lead to misdiagnosis, thus underestimating the actual global impact of the disease. The present study describes the [...] Read more.
Toxocariasis is a widespread zoonotic parasitic disease with a significant socioeconomic impact, particularly on underprivileged communities. Limitations of existing diagnostic tools and vague presenting symptoms may lead to misdiagnosis, thus underestimating the actual global impact of the disease. The present study describes the isolation and production of novel recombinant monoclonal antibodies against Toxocara canis recombinant TES-26 antigen (rTES-26) utilizing a human helminth scFv phage display library. The isolated antibody clones were characterized based on their gene sequences and binding characteristics. Three clones representing unique gene families (clone 48: IgHV3-LV1; clone 49: IgHV3-LV3; clone 50: IgHV6-LV3) were isolated, but only clones 48 and 49 showed successful insertion of the full-length scFv antibody sequence after sub-cloning. Both clones produced antibody proteins of good solubility and satisfactory yield and purity. Binding assays via Western blot and ELISA using rTES-26 and Toxocara canis native protein showed that both monoclonal antibodies were highly specific and sensitive to the target antigen. A preliminary antigen detection ELISA showed the diagnostic potential of the monoclonal antibody proteins. The proteins can also be useful in studying host–parasite interactions and therapeutic applications. Full article
(This article belongs to the Special Issue Host-Pathogen Interactions and Monoclonal Antibody Therapeutics)
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8 pages, 924 KiB  
Case Report
Impact of Treatment with Ustekinumab on Severe Infections in a Patient with Uncontrolled Psoriasis and Late-Onset Combined Primary Immunodeficiency: Case Report
by Luiz Euribel Prestes-Carneiro, Marilda Aparecida Milanez Morgado de Abreu, Eduardo Vinicius Mendes Roncada, Diego Garcia Muchon, Fernanda Miranda Caliani and Dewton Moraes Vasconcelos
Pathogens 2023, 12(9), 1156; https://doi.org/10.3390/pathogens12091156 - 12 Sep 2023
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Abstract
A 35-year-old man with a late-onset combined immunodeficiency (LOCID) variant of common variable immunodeficiency, severe plaque psoriasis, psoriatic arthritis, and Crohn’s disease was attended in the Regional Hospital of Presidente Prudente and HC-FMUSP, São Paulo, Brazil. Anti-IL-12/IL-23 (ustekinumab) monoclonal antibody was prescribed due [...] Read more.
A 35-year-old man with a late-onset combined immunodeficiency (LOCID) variant of common variable immunodeficiency, severe plaque psoriasis, psoriatic arthritis, and Crohn’s disease was attended in the Regional Hospital of Presidente Prudente and HC-FMUSP, São Paulo, Brazil. Anti-IL-12/IL-23 (ustekinumab) monoclonal antibody was prescribed due to the failure of other treatments (phototherapy, oral acitretin) for psoriasis and a Psoriasis Area Severity Index >10. We evaluated the impact of treatment with ustekinumab on severe infectious diseases in a patient with uncontrolled psoriasis and LOCID followed for 8 years. Four quarterly doses of ustekinumab 90 mg and human immunoglobulin replacement (10,000 mg at 28-day intervals) were administered. Immunophenotyping, cultures of lymphocytes, genetic sequencing, and whole exome sequencing were performed to investigate the primary immunodeficiency. Normal lymphocyte proliferation; pathogenic variants in genetic sequencing, and clinically significant variants in the whole exome for primary immunodeficiencies were not detected. The main infections before and after treatment with ustekinumab were chronic sinusitis and gastroenteritis. The patient was infected with COVID-19, dengue (twice) and influenza and was hospitalized three times for intravenous antibiotic therapy. Ustekinumab did not influence the susceptibility of the patient with LOCID to severe infections and significantly improved psoriasis, psoriatic arthritis, and Crohn’s disease. Full article
(This article belongs to the Special Issue Host-Pathogen Interactions and Monoclonal Antibody Therapeutics)
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