D-Index & Metrics Best Publications
Irina Caminschi

Irina Caminschi

Monash University
Australia

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Immune system
  • Cytokine

Her primary areas of study are Antigen, Cell biology, CD8, Immunology and Cytotoxic T cell. The study incorporates disciplines such as Receptor and Immune system in addition to Antigen. Her Cell biology research incorporates elements of Acquired immune system, Spectrin, T cell, Dendritic cell and Spleen.

Irina Caminschi works mostly in the field of CD8, limiting it down to concerns involving Virology and, occasionally, Monoclonal antibody. Her study in the field of Follicular dendritic cells, Orthomyxoviridae and Virus also crosses realms of CpG site. She is interested in Antigen presentation, which is a field of Cytotoxic T cell.

Her most cited work include:

  • Cross-presentation of viral and self antigens by skin-derived CD103 + dendritic cells (564 citations)
  • Mouse Plasmacytoid Cells Long-lived Cells, Heterogeneous in Surface Phenotype and Function, that Differentiate Into CD8+ Dendritic Cells Only after Microbial Stimulus (361 citations)
  • The dendritic cell subtype restricted C-type lectin Clec9A is a target for vaccine enhancement (356 citations)

What are the main themes of her work throughout her whole career to date?

Irina Caminschi mainly focuses on Immunology, Antigen, Cell biology, Cytotoxic T cell and CD8. Her Antigen study integrates concerns from other disciplines, such as T cell, Immune system, Antigen presentation, Adjuvant and Antibody. Her studies deal with areas such as Acquired immune system, Cross-presentation, Antigen-presenting cell, Dendritic cell and Receptor as well as Cell biology.

As a part of the same scientific study, Irina Caminschi usually deals with the Dendritic cell, concentrating on Cell membrane and frequently concerns with Spectrin, Actin cytoskeleton, Cytoskeleton and Actin. Irina Caminschi has researched Cytotoxic T cell in several fields, including Cytokine and Interleukin 10. Her study in CD8 is interdisciplinary in nature, drawing from both Epitope, Adoptive cell transfer, In vivo and Virology.

She most often published in these fields:

  • Immunology (85.25%)
  • Antigen (85.25%)
  • Cell biology (54.92%)

What were the highlights of her more recent work (between 2018-2021)?

  • Antigen (85.25%)
  • Cell biology (54.92%)
  • CD8 (54.92%)

In recent papers she was focusing on the following fields of study:

The scientist’s investigation covers issues in Antigen, Cell biology, CD8, T cell and Cytotoxic T cell. Her studies in Cell biology integrate themes in fields like Receptor, Cross-presentation and Oligonucleotide. CD8 is a subfield of Immune system that Irina Caminschi studies.

Her T cell research is multidisciplinary, incorporating perspectives in Dendritic cell and Priming. Her Cytotoxic T cell research includes elements of Epitope and Adjuvant, Immunology, Vaccination. Her study in the field of Virus and Malaria is also linked to topics like Liver stage and Front line.

Between 2018 and 2021, her most popular works were:

  • Classical Type 1 Dendritic Cells Dominate Priming of Th1 Responses to Herpes Simplex Virus Type 1 Skin Infection. (10 citations)
  • Classical Type 1 Dendritic Cells Dominate Priming of Th1 Responses to Herpes Simplex Virus Type 1 Skin Infection. (10 citations)
  • Glycolipid-peptide vaccination induces liver-resident memory CD8+ T cells that protect against rodent malaria. (9 citations)

In her most recent research, the most cited papers focused on:

  • Gene
  • Immune system
  • Cytokine

Irina Caminschi mainly investigates Priming, Antigen presentation, CD8, Cellular differentiation and T cell. Her Priming research is multidisciplinary, relying on both Spleen, DC-SIGN, Follicular dendritic cells, Cell biology and Cell type. Irina Caminschi interconnects Virology, Epitope, Antibody, Cytotoxic T cell and Plasmodium berghei in the investigation of issues within CD8.

Her research ties Antigen and Plasmodium berghei together. Her Antigen study combines topics from a wide range of disciplines, such as Immunity and Vaccination. Irina Caminschi combines subjects such as Immunology, Virus, Herpes simplex virus, Dendritic cell and Interferon gamma with her study of Cellular differentiation.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Cross-presentation of viral and self antigens by skin-derived CD103 + dendritic cells

Sammy Bedoui;Paul G Whitney;Jason Waithman;Jason Waithman;Liv Eidsmo.
Nature Immunology (2009)

798 Citations

Mouse Plasmacytoid Cells Long-lived Cells, Heterogeneous in Surface Phenotype and Function, that Differentiate Into CD8+ Dendritic Cells Only after Microbial Stimulus

Meredith O’Keeffe;Hubertus Hochrein;David Vremec;Irina Caminschi.
Journal of Experimental Medicine (2002)

557 Citations

The dendritic cell subtype restricted C-type lectin Clec9A is a target for vaccine enhancement

Irina Caminschi;Anna I Proietto;Fatma Ahmet;Susie Kitsoulis.
Blood (2008)

497 Citations

The Dendritic Cell Receptor Clec9A Binds Damaged Cells via Exposed Actin Filaments

Jian Guo Zhang;Jian Guo Zhang;Peter E. Czabotar;Peter E. Czabotar;Antonia N. Policheni;Antonia N. Policheni;Irina Caminschi;Irina Caminschi;Irina Caminschi.
Immunity (2012)

331 Citations

CD103+ pulmonary dendritic cells preferentially acquire and present apoptotic cell–associated antigen

A. Nicole Desch;Gwendalyn J. Randolph;Kenneth M Murphy;Emmanuel L Gautier.
Journal of Experimental Medicine (2011)

319 Citations

Liver-Resident Memory CD8 + T Cells Form a Front-Line Defense against Malaria Liver-Stage Infection.

Daniel Fernandez-Ruiz;Wei Yi Ng;Wei Yi Ng;Lauren E Holz;Joel Z Ma.
Immunity (2016)

317 Citations

Comparable T helper 1 (Th1) and CD8 T-cell immunity by targeting HIV gag p24 to CD8 dendritic cells within antibodies to Langerin, DEC205, and Clec9A

Juliana Idoyaga;Ashira Lubkin;Christopher Fiorese;Mireille H. Lahoud;Mireille H. Lahoud.
Proceedings of the National Academy of Sciences of the United States of America (2011)

306 Citations

Targeting Antigen to Mouse Dendritic Cells via Clec9A Induces Potent CD4 T Cell Responses Biased toward a Follicular Helper Phenotype

Mireille H. Lahoud;Fatma Ahmet;Susie Kitsoulis;Soo San Wan.
Journal of Immunology (2011)

213 Citations

C-Rel Regulates Interleukin 12 P70 Expression in Cd8+ Dendritic Cells by Specifically Inducing p35 Gene Transcription

Raelene Grumont;Hubertus Hochrein;Meredith O'Keeffe;Raffi Gugasyan.
Journal of Experimental Medicine (2001)

203 Citations

Production of interferons by dendritic cells, plasmacytoid cells, natural killer cells, and interferon-producing killer dendritic cells.

David Vremec;Meredith O'Keeffe;Hubertus Hochrein;Martina Fuchsberger.
Blood (2007)

171 Citations

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