Hydrogen Therapy in Lung CancerScientific Research

The Original Article:

original title: Two weeks of hydrogen inhalation can significantly reverse adaptive and innate immune system senescence patients with advanced non-small cell lung cancer: a self-controlled study

Published: 2020 Year

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Original Publication

INTRODUCTION

The recurrence and metastasis of malignant tumors are difficult to control, which can be attributed to three main reasons: 1) immunosenescence; 2) tumor-associated factors; and 3) cancer therapy itself.¹ Immunosenescence is characterized by the gradual deterioration of the immune system during the natural ageing process. A long-term tumor-bearing state will also lead to the exhaustion and senescence of cytotoxic lymphocytes, including T cells, natural killer (NK) cells, NKT cells, and gamma delta (γδ) T cells.²³ Tumor factors are associated with an excessive tumor burden and severely inhibited immune function, including increased CD4⁺ CD25⁺ regulatory T cells.⁴ Currently, a variety of conventional treatments have been shown to accelerate the recurrence and metastasis of residual tumors, including surgery,⁵ radiation,⁶ chemotherapy,⁷ and even general anesthesia.⁸

Of all cancers, lung cancer is associated with the highest incidence throughout the world, of which non-small cell lung cancer (NSCLC) accounts for approximately 85% of cases.⁹ Due to the lack of early symptoms for lung cancer, many patients are in an advanced stage at the time of diagnosis, and survival time is typically with 1 year.¹⁰ Studies have shown that nearly 27% of patients who underwent surgery and chemotherapy died from recurrence and metastasis.¹¹ Thus, immune reconstruction, both before or after standard therapies, is a necessary method for prolonging the survival of cancer patients who are in an advanced stage.¹² The current strategies of immune reconstruction primarily include adoptive immune cell supplementation, specific or non-specific immune activators, cancer vaccines, and exercise.¹³ As an antioxidant gas, hydrogen can diffuse into the mitochondria of lymphocytes and selectively neutralize oxygen free radicals.¹⁴¹⁵ Moreover, hydrogen inhalation has been verified to reduce PD-1 expression, a marker of cell exhaustion,¹⁶ on the surface of cytotoxic T cells in patients with advanced colorectal cancer, which prolongs progression-free survival and overall survival.¹⁷ In this study, immunosenescence in advanced NSCLC patients was tested, and hydrogen inhalation was used to reverse the immunosenescence while patients were awaiting treatment.

SUBJECTS AND METHODS

Subjects

Between July and September 2019, 20 advanced NSCLC patients who hospitalized at Fuda Cancer Hospital and needed to wait 2 weeks for treatment were enrolled in this self-controlled study. According to the registered clinical trial (ClinicalTrials.gov, ID: NCT03818347; Registration Date: January 24, 2019), the inclusion criteria consisted of: stage III or IV NSCLC diagnosed by imaging and pathology¹⁸; tumor number 1–6; maximum tumor length < 2 cm; Karnofsky performance status (KPS) score ≥ 7019</sup>; expected survival time > 6 months; platelet count ≥ 80 × 109</sup>/L; white blood cell count ≥ 3 × 109</sup>/L; neutrophil count ≥ 2 × 109</sup>/L; and hemoglobin ≥ 80 g/L. The exclusion criteria consisted of patients with a cardiac pacemaker, brain metastasis, grade 3 hypertension or diabetic complication, severe cardiac and pulmonary dysfunction. None of the patients received any standard treatment during the hydrogen inhalation period.</sup>

Ethical statement

The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. The study protocol received ethical approval from the Ethics Committee of Fuda Cancer Hospital, Jinan University in China (approval No. Fuda20181207) on December 7, 2018. Written informed consent was obtained from each participant in accordance with the Declaration of Helsinki.

Hydrogen inhalation method

Hydrogen was produced by a hydrogen-oxygen nebulizer (AMS-H-03, Shanghai Asclepius Meditec Co., Ltd., Shanghai, China). The patients remained seated or recumbent, and inhaled a mixture of hydrogen (66.7%) and oxygen (33.3%) via a nasal tube or mask with a gas flow rate of 3 L/min. The hydrogen inhalation was continued for 4 hours per day for 2 weeks in a specialized treatment facility.

Pulmonary symptoms and KPS score

Before and after hydrogen therapy, the respiratory function was assessed by very experienced respiratory physicians using a pulmonary function tester (Autospiro AS-507; Minato Medical Science, Tokyo, Japan), pulmonary tumor-related symptoms and the KPS score were evaluated by resident doctors in charge.

Immunophenotype evaluation

Approximately 5 mL of peripheral blood was extracted from elbow of all enrolled patients before hydrogen inhalation, as well as at one and two weeks after hydrogen inhalation. Peripheral blood monocyte cells were isolated using a Ficoll solution and labeled with fluorescent antibodies (BD Biosciences, San Jose, CA, USA). T lymphocytes, NK, NKT, and γδ T cells were analyzed using flow cytometry (FACSanto II; BD Biosciences, San Jose, CA, USA) by a professional third-party inspection center (Shuangzhi Purui Medical Laboratory Co., Ltd., Wuhan, Hubei Province, China).

Statistical analysis

The calculation method of sample size is based on MedSci Sample Size tools (MSST) software (MedSci, Shanghai, China). Pulmonary symptoms before and after hydrogen inhalation were compared using paired t-test. Respiratory function, KPS score, and immunoassays were compared by repeated measures analysis of variance and Bonferroni’s multiple comparison test. Statistical differences were indicated by P < 0.05. All analyses and figures were produced using GraphPad Prism 5.0 (GraphPad software, San Diego, CA, USA).

RESULTS

Clinical data of NSCLC patients

A total of 20 consecutive patients admitted to the hospital participated in this study. The clinicopathological data are listed in Table 1.

Changes in the KPS score and pulmonary symptoms of NSCLC patients

All patients underwent hydrogen inhalation for 2 weeks, with no treatment-related discomfort or side effects. The results regarding respiratory function, KPS score, and pulmonary symptoms before and 2 weeks after hydrogen therapy are presented in Table 2. At the end of hydrogen treatment, fewer people with different lung symptoms, with a statistical reduction in those with moderate cough and mild dyspnea.

Changes in T cell subsets of NSCLC patients undergoing hydrogen therapy

This portion of the test consisted of three parts: CD4⁺ T cells, CD8⁺ T cells, and cytokine-secreting helper T (Th) cells. Before the initiation of hydrogen therapy, six primary immunosenescence indexes were identified. Among these indexes, the abnormally lower indexes included a percentage of functional helper and cytotoxic T cells, Th1, and follicular Th cells; the abnormally higher indexes were associated with the percentage of exhausted and senescent cytotoxic T cells (Figure 1). For the CD4⁺ subsets, functional Th cells increased to within the normal range after one week of hydrogen inhalation and increased significantly after 2 weeks (P < 0.05). Both exhausted Th cell and regulatory T cells decreased gradually (both P < 0.05) after 2 weeks of hydrogen therapy (Figure 1A). For the CD8⁺ subsets, functional cytotoxic T cells increased to within the normal range after 2 weeks of hydrogen inhalation (P < 0.05); both exhausted and senescent cytotoxic T cells decreased gradually to within the normal range (both P < 0.05) after 2 weeks of therapy (Figure 1B). For the cytokine-secreting Th subsets, only Th1 cells increased gradually near normal range after 2 weeks of hydrogen inhalation therapy (P < 0.05; Figure 1C). No other cells changed significantly within 2 weeks of hydrogen inhalation.

Changes in NKT and NK cells of NSCLC patients undergoing hydrogen therapy

Before the start of hydrogen therapy, the percentage of total NKT cell, activated NK and killer NK subsets was all below the normal range (Figure 2). One week after hydrogen inhalation, the activated NK cell subset increased to within the normal range (Figure 2C). Two weeks later, both the total NKT and killer NK subsets were higher than the percentage before treatment (both P < 0.05; Figure 2A and D), and activated NK cells were significantly elevated (P < 0.01; Figure 2C). Total NK cells did not change significantly within 2 weeks of hydrogen inhalation (Figure 2B).

Changes in γδ T cell subsets of NSCLC patients undergoing hydrogen therapy

TBefore the start of hydrogen therapy, the percentage of both Vδ1 cell and killer Vδ1 cell was higher than the normal range, and the percentage of Vδ2 cell was below the normal range (Figure 3). One week after hydrogen inhalation, the percentage of Vδ2 cell in γδ T cells rose to within the normal range (Figure 3C). Two weeks later, the total γδ T cells and Vδ2 cells was higher than the percentage before treatment (both P < 0.05; Figure 3A and C), exhausted Vδ2 cell was lower than that before treatment (P < 0.05; Figure 3C</a>); exhausted Vδ1 cell decreased significantly (P < 0.001; Figure 3B), and killer Vδ2 cell increased significantly (P < 0.01; Figure 3C). No other cells changed significantly within 2 weeks of hydrogen inhalation.

DISCUSSION

Although a connection between immunodeficiency and oncogenesis has been proposed, a detailed immune profile in cancer has not yet been described in sufficient detail. It is well-known that the immune system deteriorates with cancer progression as a consequence of decreasing levels of functional T cells, downregulation of costimulatory molecules, and expansion of memory T cells.²⁰²¹ Chen et al.²² showed that there were differences in the immune profiles between cancer patients and normal subjects; in particular, a decreased proportion of CD4⁺ and CD8⁺ T cell subsets was observed in cancer patients, especially in patients who were associated with a more advanced disease stage and those who had received conventional chemotherapy treatment. In addition, Saavedra et al.²³ reported that cancer and chemotherapy influenced the various lymphocyte subsets in NSCLC patients, in which B cells decreased with cancer disease progression, and CD28^– subpopulations (exhausted or senescent T cells) increased following chemotherapy. Our study found similar results in the adaptive immune system, which was found to be primarily due to an increase in the proportion of exhausted and senescent T cell subsets, as well as a decreased proportion of functional subsets. Moreover, we also found evidence for the weak ability of Th1 and follicular Th cells on cytokine secretion. In the detection of the innate immune response (NK, NKT, and γδ T cells), we discovered that there was a decreased proportion of NKT, activated NK and killer NK cells, and an insufficient content of Vδ2 subsets among γδ T cells. Thus, it is highly likely that the adaptive and innate immune systems jointly contribute to the progression of NSCLC.

Advanced NSCLC has many characteristics that are distinct from other cancers, including that over 65% of patients are often over 70 years old²⁴ and in most cases, the disease has progressed from early stage cancer and they have been exposed to long-term chronic antigenic stimulation.²⁵ Therefore, the immunosenescence characteristics obtained in advanced NSCLC can only be used as a reference for other cancer types. Moreover, there may be huge differences among different cancer types, which require further investigation.

Immune cell senescence focuses on the phenotypic characteristics of individual lymphocytes; however, the function does not necessarily decrease during aging.²⁶²⁷²⁸ In contrast, immune cell exhaustion is due to the presence of excessive free radicals in the mitochondria, which results in a loss of function and induces programmed apoptosis.²⁹ Senescence and exhaustion are not simply the result of an inevitable and progressive decline of all immune functions, but rather represent a highly dynamic process of remodeling and adaptation.³⁰ Thus, we attempted to rescue the function of exhausted and senescent lymphocytes with hydrogen gas, which was reported to protect the mitochondrial function of human lymphocytes.¹⁷³¹³² By comparing the immune function before and after hydrogen inhalation, we found that a period of two weeks was sufficient to reverse the multiple senescent or exhausted cell subsets into functional subsets, which had no effect on the percentage of CD4⁺ or CD8⁺ T cells. In addition to adaptive immune cells,¹⁷ both tumor killing-associated Th1 cytokines³³ and innate immune cells (i.e., NK,³⁴ NKT,³⁵ total γδ T cell,³⁶ Vδ1 cell,³⁷ and Vδ2³⁸ cell) have been found to be significantly activated following hydrogen inhalation. Surprisingly, after hydrogen therapy, the proportion of regulatory T cells in the blood decreased significantly, demonstrating that hydrogen can control tumor progress with different mechanisms.³⁹ Although the improvement in both the number and function of these cells does not necessarily reduce the size of the tumor, it may alter the systemic immunosuppressive state and the tumor microenvironment, as well as reduce tumor invasiveness. Improvements in the systemic signs and pulmonary symptoms after hydrogen inhalation in some patients are likely to validate this hypothesis.

Since most cancer patients need time to complete the admission check and wait for a specific treatment program, we should try to turn this “wasted time” into a “prime time,” in an effort to restore the immune system prior to hospital treatment. This study reports primary evidence that two weeks of hydrogen inhalation can significantly reverse the senescence of both the adaptive and innate immune system. The limitations of this paper are the small number of participants and the short time of hydrogen treatment, so the following issues remain unknown: 1) whether the duration of prolonged hydrogen inhalation can continue to improve immune function; 2) the optimal level of immune improvement; 3) whether the therapeutic effects rebound after the cessation of hydrogen inhalation; and 4) whether improving immune function before treatment will reduce tumor recurrence and metastasis. Such questions should be further investigated in future research.