Presence of B Cells in Tertiary Lymphoid Structures Is Associated with a Protective Immunity in Patients with Lung Cancer

2014 ◽  
Vol 189 (7) ◽  
pp. 832-844 ◽  
Author(s):  
Claire Germain ◽  
Sacha Gnjatic ◽  
Fella Tamzalit ◽  
Samantha Knockaert ◽  
Romain Remark ◽  
...  
Cancers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 2644
Author(s):  
Jun Tang ◽  
Daniel Ramis-Cabrer ◽  
Víctor Curull ◽  
Xuejie Wang ◽  
Mercé Mateu-Jiménez ◽  
...  

Immune profile of B and T cells and tertiary lymphoid structures (TLSs) may differ in tumors of lung cancer (LC) patients with/without chronic obstructive pulmonary disease (COPD), and may also influence patient survival. We sought to analyze: (1) TLSs, germinal centers (GCs), B and T cells, and (2) associations of the immune biomarkers with the patients’ 10-year overall survival (OS). TLSs (numbers and area), B [cluster of differentiation (CD) 20], and T (CD3), and GCs cells were identified in both tumor and non-tumor specimens (thoracotomy) from 90 LC-COPD patients and 43 LC-only patients. Ten-year OS was analyzed in the patients. Immune profile in tumors of LC-COPD versus LC: TLS numbers and areas significantly decreased in tumors of LC-COPD compared to LC patients. No significant differences were observed in tumors between LC-COPD and LC patients for B or T cells. Immune profile in tumors versus non-tumor specimens: TLS areas and B cells significantly increased, T cells significantly decreased in tumors of both LC and LC-COPD patients. Survival: in LC-COPD patients: greater area of TLSs and proportion of B cells were associated with longer survival rates. The immune tumor microenvironment differs in patients with underlying COPD and these different phenotypes may eventually impact the response to immunotherapy in patients with LC.


2021 ◽  
Author(s):  
Tullia Bruno ◽  
Dongyan Liu ◽  
Sheryl Kunning ◽  
Riyue Bao ◽  
Laura Stabile ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Marta Trüb ◽  
Alfred Zippelius

Tertiary lymphoid structures (TLS) are ectopic lymphoid formations which are formed under long-lasting inflammatory conditions, including tumours. TLS are composed predominantly of B cells, T cells and dendritic cells, and display various levels of organisation, from locally concentrated aggregates of immune cells, through clearly defined B cell follicles to mature follicles containing germinal centres. Their presence has been strongly associated with improved survival and clinical outcome upon cancer immunotherapies for patients with solid tumours, indicating potential for TLS to be used as a prognostic and predictive factor. Although signals involved in TLS generation and main cellular components of TLS have been extensively characterised, the exact mechanism by which TLS contribute to the anti-tumour response remain unclear. Here, we summarise the most recent development in our understanding of their role in cancer and in particular in the response to cancer immunotherapy. Deciphering the relationship between B cells and T cells found in TLS is a highly exciting field of investigation, with the potential to lead to novel, B-cell focused immunotherapies.


2017 ◽  
Vol 215 ◽  
pp. 74-82 ◽  
Author(s):  
Chie Sakimura ◽  
Hiroaki Tanaka ◽  
Takahiro Okuno ◽  
Soichiro Hiramatsu ◽  
Kazuya Muguruma ◽  
...  

2020 ◽  
Vol 108 (4) ◽  
pp. 1307-1318
Author(s):  
Luciana Rodrigues Carvalho Barros ◽  
Paulo Thiago De Souza‐Santos ◽  
Marco Antonio Marques Pretti ◽  
Gustavo Fioravanti Vieira ◽  
Marcelo Alves De Souza Bragatte ◽  
...  

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