Cytolytic T-cell response against Epstein-Barr virus in lung cancer patients and healthy subjects
© Karanikas et al; licensee BioMed Central Ltd. 2010
Received: 6 April 2010
Accepted: 4 June 2010
Published: 4 June 2010
This study aimed to examine whether EBV seropositive patients with lung cancer have an altered virus-specific CTL response, as compared to age-matched healthy controls and whether any variation in this response could be attributed to senescence.
Peripheral blood mononuclear cells from lung cancer patients, age-matched and younger healthy individuals were used to measure EBV-specific CTLs after in vitro amplification with the GLCTLVAML and RYSIFFDYM peptides followed by HLA-multimer staining.
Lung cancer patients and aged-matched controls had significantly lesser EBV-specific CTL than younger healthy individuals. Multimer positive populations from either group did not differ with respect to the percentage of multimer positive CTLs and the intensity of multimer binding.
This study provides evidence that patients with lung cancer exhibit an EBV-specific CTL response equivalent to that of age-matched healthy counterparts. These data warrant the examination of whether young individuals have a more robust anti-tumor response, as is the case with the anti-EBV response.
Evidence suggests that cancer patients present with a compromised immune response of multifactorial origin, including the tumor itself. It seems that the early stages of tumor growth appear not to elicit systemic immune deficiency and are sometimes associated with antigen-specific tolerance, while generalized immunodeficiency can arise during the late stages of tumor development . Related data are mainly derived either from in vitro experiments or from DTH measurements in the context of cancer immunotherapy . Therefore, the existing evidence remains inconclusive, while the significance of the described immune alterations in relation to the ability of cancer patients to mount effective responses against pathogens has not been clarified. Finally, there is existing controversy regarding the efficacy of influenza vaccination in patients with cancer [3, 4].
This study was scheduled in order to examine whether, at diagnosis, EBV seropositive patients with lung cancer, have a compromised virus-specific CTL response, as compared to age-matched healthy controls. A group of younger healthy individuals was also examined to ascertain whether a possible reduction in the anti-EBV CTL responses of the above patients and age-matched controls could be attributed to senescence. Lung cancer was selected because although such cancers express several tumour antigens  and T cells infiltrating these tumours have been identified , the outcomes of specific immunotherapy for patients with lung cancer is rather poor .
Subjects and methods
Patients and controls
PBMC were isolated from whole blood collected at diagnosis from 19 patients with primary lung cancer. Thirteen of them were diagnosed with NSCLC (mean age 66.8 ± 11.8 years; 3 females, 10 males) and the remaining 6 with SCLC (mean age 67.0 ± 7.4 years; 1 female, 5 males). PBMC were also collected from 14 age-matched healthy individuals (mean age 58.2 ± 5.8 years; 4 females, 10 males) as well as from 7 healthy younger individuals (mean age 26.7 ± 1.0 years; 4 females, 3 males). All PBMC were kept frozen till required. Subjects expressed HLA-A2 and/or -A24 (patients: 11 HLA-A2, 6 HLA-A24, 2 HLA-A2/-A24; age-matched healthy individuals: 8 HLA-A2, 5 HLA-A24, 1 HLA-A2/-A24; young healthy individuals: 5 HLA-A2, 2 HLA-A2/-A24) and there were positive for IgG antibodies against the EBV nuclear antigen 3C (EBNA3C). The study conforms to the provisions of the Declaration of Helsinki, it was reviewed and approved by the University of Thessaly Ethics Committee, and all participants provided informed consent.
Detection of EBV-specific CTLs
Peptide-specific CTLs were detected using HLA-multimer flow cytometry after a previous step of in vitro amplification of MLPCs with peptides under limiting dilution conditions, exactly as described in detail previously . Two EBV peptides, GLCTLVAML (BMLF1.A2 presented by HLA-A2) and RYSIFFDYM (EBNA3C.A24 presented by HLA-A24) were used. These were synthesized on solid phase using F-moc for transient NH2-terminal protection, purchased as lyophilised at > 90% purity ascertained by mass spectrometry (Abgent, San Diego, USA), dissolved in DMSO at 10 mg/mL, and stored at -20 °C before use. Specific multimers labelled with APC and control multimers with PE were used to stain MLPC. Each MLPC was considered to contain a multimer positive population, only if staining with the specific HLA-multimer resulted in a distinct cell cluster that did not stain with control HLA-multimers of different specificity.
Results are expressed as mean ± SD and were analyzed using two tailed chi-square analysis without Yate's correction. The level of significance was 0.05 (two-sided). The commercially available statistical software (SPSS for Windows, release 14.0; SPSS Inc., Chicago, IL.) was used.
Anti-CMV serological response amongst each group
Mean ± Standard deviationa
Young healthy individuals
267 ± 183
Young vs Aged: 0.049
Aged healthy individuals
377 ± 83
Young vs Patients: 0.466
Patients with lung cancer
341 ± 199
Aged vs Patients: 0.024
Number of EBV specific CTL amongst each group
Mean ± Standard deviationa
Young healthy individuals
24.3 ± 17.9
3.1 - 54.8
Aged healthy individuals
25.2 ± 17.2
10.4 - 53.9
Patients with lung cancer
21.8 ± 18.7
1.9 - 60.2
Correlations of anti-EBV T cell response upon diagnosis with clinicopathological parameters
Anti-EBV T cell responsea
Performance Status d
Loss of weight
843.88 ± 235.59
757.89 ± 292.30
This study provides direct evidence that lung cancer patients dispose an EBV-specific CTL response equivalent to that of age-matched healthy counterparts. Moreover, it was demonstrated that the EBV-specific CTL response mounted by subjects of this age group, either with cancer or not, was twice as less than that elicited by younger healthy individuals. Regarding the healthy individuals, our results are in accordance to those reported recently by Colonna-Romano et al  demonstrating an inverse correlation between age and the percentage of circulating EBV-specific CTLs. Most likely, these observations can be explained in the context of the complex process of T cell immunosenescence [9, 12].
With respect to cancer patients, it is interesting that they present with the same age-related alteration of EBV-specific CTL response as their healthy counterparts. In other words, neither the antigenic burden of the tumor nor any other cancer-related factor affected their ability to mount a CTL response against the virus. Assuming that the CTL response of cancer patients against other pathogens follows a similar pattern of alterations, no special vaccination strategy  is required other than that followed for elderly people in general, except when they are under the influence of immunosuppressive therapies. To this end, it must be noted that considering the low frequencies detected in our study population (3-60/million CD8), one has no other alternative but to attempt to amplify these cells first in order to understand their reactivity. This is not unusual since other we and others have confirmed that in most cases CTL responses detected after in vitro stimulation reflect the true number of these cells circulating in vivo [13, 14].
Beyond differences observed in the specific pCTL frequency related to age, cancer patients also appeared with a decreased proliferative capacity of virus specific pCTL. Most likely these differences could be explained by replicative senescence [15, 16], whereby viral specific CTL in patients have multiplied several times over their lifetime and present with a reduced ability to further respond to an antigenic stimulus. This does not exclude their presence but rather supports the fact that T cell clonal exhaustion results in the accumulation of oligoclonal dysfunctional cells followed by repertoire shrinkage due to clonal deletion, maintaining however, the actual number of dysfunctional cells , as has recently being demonstrated in patients with renal cell cancer .
Many investigators relate the immune dysfunction of cancer patients with both the inefficient anti-tumor response and a reduced efficacy of immunotherapy [19, 20]. To this end, we have recently identified that patients with lung cancer present with a tenfold higher number of anti-tumor CTL as compared to the age-matched controls . These results suggest that such patients do not have an immunocompromised CD8 T cell response but the ineffective anti-tumor response, is most likely a reflection of the age-associated changes that take place in individuals  impacting on their capacity to respond effectively against the tumor. Under the light of the data presented herein, it is worth examining whether young individuals have a more robust anti-tumor response, as is the case with the anti-EBV response.
In conclusion, this study provides evidence that lung cancer patients dispose an EBV-specific CTL response equivalent to that of age-matched healthy counterparts. Our study suggests that possibly the poor outcome of cancer immunotherapeutic approaches in lung cancer can be a result of the underlying effects of senescence on the immune system rather than an inefficient anti-tumor response. These data warrant the examination of whether young individuals have a more robust anti-tumor response, as is the case with the anti-EBV response.
This work was supported by (a) a European Union - European Social Fund (75%) and the Greek Ministry of Development-GSRT (25%) (ENTER 04EP09) grant and (b) a Marie Curie Incoming International Fellowship within the 6th European Community Framework Programme (FP6 Contract MIF1-CT-2006-021795, IRTALUNG) grant.
List of Abbreviations
cytolytic CD8+ T cell
mixed lymphocyte-peptide cultures
non-small cell lung carcinoma
peripheral blood mononuclear cells
small cell lung carcinoma
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