<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Martín-Ruiz, Asunción</dc:creator>
  <dc:creator>Fiuza-Luces, Carmen</dc:creator>
  <dc:creator>Martínez-Martínez, Esther</dc:creator>
  <dc:creator>Arias, Clemente F.</dc:creator>
  <dc:creator>Gutiérrez, Lourdes</dc:creator>
  <dc:creator>Ramírez, Manuel</dc:creator>
  <dc:creator>Martín-Acosta, Paloma</dc:creator>
  <dc:creator>Coronado, Maria José</dc:creator>
  <dc:creator>Lucia, Alejandro</dc:creator>
  <dc:creator>Provencio, Mariano</dc:creator>
  <dc:date>2020-04-27</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Immunotherapies, such as checkpoint blockade of programmed cell death  protein-1 (PD-1), have resulted in unprecedented improvements in survival for  patients with lung cancer. Nonetheless, not all patients benefit equally and  many issues remain unresolved, including the mechanisms of action and the  possible effector function of immune cells from non-lymphoid lineages. The  purpose of this study was to investigate whether anti-PD-1 immunotherapy acts  on malignant tumor cells through mechanisms beyond those related to T  lymphocyte involvement. We used a murine patient-derived xenograft (PDX)  model of early-stage non–small cell lung carcinoma (NSCLC) devoid of host  lymphoid cells, and studied the tumor and immune non-lymphoid responses to  immunotherapy with anti-PD-1 alone or in combination with standard  chemotherapy (cisplatin). An antitumor effect was observed in animals that  received anti-PD-1 treatment, alone or in combination with cisplatin, likely due  to a mechanism independent of T lymphocytes. Indeed, anti-PD-1 treatment  induced myeloid cell mobilization to the tumor concomitant with the production  of exudates compatible with an acute inflammatory reaction mediated by murine  polymorphonuclear leukocytes, specifically neutrophils. Thus, while keeping in  mind that more research is needed to corroborate our findings, we report  preliminary evidence for a previously undescribed immunotherapy mechanism  in this model, suggesting a potential cytotoxic action of neutrophils as PD-1  inhibitor effector cells responsible for tumor regression by necrotic extension.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/308586</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308586/files/mar_eap.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308586/files/mar_eap_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1038/s41598-020-63796-w</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Scientific Reports. - 2020, vol. 10, no. 1, p. 7078</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Effects of anti-PD-1 immunotherapy on tumor regression: insights from a patient-derived xenograft model</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
