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Antibodies from Sierra Leonean and Nigerian Lassa fever survivors cross-react with recombinant proteins representing Lassa viruses of divergent lineages.
Heinrich, Megan L; Boisen, Matthew L; Nelson, Diana K S; Bush, Duane J; Cross, Robert W; Koval, Anatoliy P; Hoffmann, Andrew R; Beddingfield, Brandon J; Hastie, Kathryn M; Rowland, Megan M; Aimukanova, Irina; Koval, Sophia; Lathigra, Raju; Borisevich, Viktoriya; Momoh, Mambu; Sandi, John Demby; Goba, Augustine; Odia, Lkponmwosa; Baimba, Francis; Aiyepada, John O; Ebo, Benevolence; Eromon, Philomena; Ugwu, Chinedu; Folarin, Onikepe; Olumade, Testimony; Onyechi, MacDonald N; Etafo, Johnson; Adeyemi, Rashidat; Ella, Elijah E; Aminu, Maryam; Gomerep, Simji S; Eke, Matthew Afam; Ogunsanya, Olusola; Akpede, George O; Asogun, Danny O; Okogbenin, Sylvanus A; Okokhere, Peter O; Holst, Johan; Shaffer, Jeffrey G; Schieffelin, John S; Geisbert, Thomas W; Saphire, Erica Ollmann; Happi, Christian T; Grant, Donald S; Garry, Robert F; Branco, Luis M.
Affiliation
  • Heinrich ML; Zalgen Labs, LCC, Germantown, MD, USA.
  • Boisen ML; Zalgen Labs, LCC, Germantown, MD, USA.
  • Nelson DKS; Zalgen Labs, LCC, Germantown, MD, USA.
  • Bush DJ; Zalgen Labs, LCC, Germantown, MD, USA.
  • Cross RW; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
  • Koval AP; Galveston National Laboratory, Galveston, TX, USA.
  • Hoffmann AR; Zalgen Labs, LCC, Germantown, MD, USA.
  • Beddingfield BJ; Department of Microbiology and Immunology, School of Medicine, Tulane University, 1430 Tulane Avenue, New Orleans, LA, JBJ56870118, USA.
  • Hastie KM; Department of Microbiology and Immunology, School of Medicine, Tulane University, 1430 Tulane Avenue, New Orleans, LA, JBJ56870118, USA.
  • Rowland MM; La Jolla Institute for Immunology, La Jolla, CA, 92037, USA.
  • Aimukanova I; Zalgen Labs, LCC, Germantown, MD, USA.
  • Koval S; Zalgen Labs, LCC, Germantown, MD, USA.
  • Lathigra R; Zalgen Labs, LCC, Germantown, MD, USA.
  • Borisevich V; Zalgen Labs, LCC, Germantown, MD, USA.
  • Momoh M; Galveston National Laboratory, Galveston, TX, USA.
  • Sandi JD; Department of Pathology, University of Texas Medical Branch, Galveston, TX, USA.
  • Goba A; Eastern Polytechnic Institute, Kenema, Sierra Leone.
  • Odia L; Viral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone.
  • Baimba F; Ministry of Health and Sanitation, Freetown, Sierra Leone.
  • Aiyepada JO; Viral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone.
  • Ebo B; Viral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone.
  • Eromon P; Institute of Lassa Fever Research and Control, Irrua Specialist Teaching Hospital, Irrua, Edo State, Nigeria.
  • Ugwu C; Viral Hemorrhagic Fever Program, Kenema Government Hospital, Kenema, Sierra Leone.
  • Folarin O; Institute of Lassa Fever Research and Control, Irrua Specialist Teaching Hospital, Irrua, Edo State, Nigeria.
  • Olumade T; Institute of Lassa Fever Research and Control, Irrua Specialist Teaching Hospital, Irrua, Edo State, Nigeria.
  • Onyechi MN; The African Center of Excellence for Genomics of Infectious Diseases, Redeemer's University, Ede, Osun State, Nigeria.
  • Etafo J; Department of Biological Sciences, College of Natural Sciences, Redeemer's University, Ede, Osun State, Nigeria.
  • Adeyemi R; The African Center of Excellence for Genomics of Infectious Diseases, Redeemer's University, Ede, Osun State, Nigeria.
  • Ella EE; Department of Biological Sciences, College of Natural Sciences, Redeemer's University, Ede, Osun State, Nigeria.
  • Aminu M; The African Center of Excellence for Genomics of Infectious Diseases, Redeemer's University, Ede, Osun State, Nigeria.
  • Gomerep SS; Department of Biological Sciences, College of Natural Sciences, Redeemer's University, Ede, Osun State, Nigeria.
  • Eke MA; The African Center of Excellence for Genomics of Infectious Diseases, Redeemer's University, Ede, Osun State, Nigeria.
  • Ogunsanya O; Department of Biological Sciences, College of Natural Sciences, Redeemer's University, Ede, Osun State, Nigeria.
  • Akpede GO; Federal Medical Center Owo, Owo, Nigeria.
  • Asogun DO; Federal Medical Center Owo, Owo, Nigeria.
  • Okogbenin SA; Ahmadu Bello University, Zaria, Nigeria.
  • Okokhere PO; Ahmadu Bello University, Zaria, Nigeria.
  • Holst J; Ahmadu Bello University, Zaria, Nigeria.
  • Shaffer JG; University Teaching Hospital, Jos, Nigeria.
  • Schieffelin JS; Federal Medical Center, Abakaliki, Nigeria.
  • Geisbert TW; University of Ibadan, Ibadan, Nigeria.
  • Saphire EO; Institute of Lassa Fever Research and Control, Irrua Specialist Teaching Hospital, Irrua, Edo State, Nigeria.
  • Happi CT; Department of Paediatrics, Irrua Specialist Teaching Hospital, Irrua, Nigeria.
  • Grant DS; Department ofPaediatrics, College of Medicine, Ambrose Alli University, Ekpoma, Nigeria.
  • Garry RF; Institute of Lassa Fever Research and Control, Irrua Specialist Teaching Hospital, Irrua, Edo State, Nigeria.
  • Branco LM; Department of Community Medicine, Irrua Specialist Teaching Hospital, Irrua, Nigeria.
Sci Rep ; 10(1): 16030, 2020 09 29.
Article in En | MEDLINE | ID: mdl-32994446
ABSTRACT
Lassa virus (LASV) is the causative agent of Lassa fever, an often-fatal hemorrhagic disease that is endemic in West Africa. Seven genetically distinct LASV lineages have been identified. As part of CEPI's (Coalition for Epidemic Preparedness Innovations) Lassa vaccine development program, we assessed the potential of the human immune system to mount cross-reactive and cross-protective humoral immune responses to antigens from the most prevalent LASV lineages, which are lineages II and III in Nigeria and lineage IV in Sierra Leone. IgG and IgM present in the blood of Lassa fever survivors from Nigeria or Sierra Leone exhibited substantial cross-reactivity for binding to LASV nucleoprotein and two engineered (linked and prefusion) versions of the glycoproteins (GP) of lineages II-IV. There was less cross-reactivity for the Zinc protein. Serum or plasma from Nigerian Lassa fever survivors neutralized LASV pseudoviruses expressing lineage II GP better than they neutralized lineage III or IV GP expressing pseudoviruses. Sierra Leonean survivors did not exhibit a lineage bias. Neutralization titres determined using LASV pseudovirus assays showed significant correlation with titres determined by plaque reduction with infectious LASV. These studies provide guidance for comparison of humoral immunity to LASV of distinct lineages following natural infection or immunization.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cross Reactions / Lassa Fever / Lassa virus Limits: Humans Country/Region as subject: Africa Language: En Journal: Sci Rep Year: 2020 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cross Reactions / Lassa Fever / Lassa virus Limits: Humans Country/Region as subject: Africa Language: En Journal: Sci Rep Year: 2020 Document type: Article Affiliation country: