Abstract
Two attempts to address health issues by indoor environment modifications are introduced. One approach involves enhancement of natural killer cell activity by negatively charged particle dominant indoor air conditions (NCPDIAC) resulting from extra-porous charcoal paint and application of an electric voltage on the wall surface to adsorb positively charged small particles (approx. 20 nm in diameter). This apparatus creates relatively continuous NCPDIAC. The other approach involves prevention of pollen allergy symptoms by a cloth containing specific ore powder (CCSNOP). With the former approach, we engaged in short-term (2.5 hour), middle-term (2 W night stay), and long-term (3 M) stays under NCPDIAC and found that IL-2 levels increased under short-term stays and that natural killer cell activity was enhanced in middle- and long-term stay experiments. Implementation of this strategy may partially prevent the occurrence of cancers and viral-mediated diseases. With the latter approach, a 1-hour stay within a CCSNOP room resulted in improvement of symptoms in patients with pollen allergies in addition to a reduction in bad moods caused by any remaining symptoms. In both cases, longer-term experiments should be performed in an effort to confirm and delineate the biological effects of these indoor environment modifications on human health problems.
Keywords
- indoor air
- negatively charged particle
- natural killer cell activity
- pollen allergy
1. Introduction
The nature of indoor environments is important in terms of human health. One typical illness related to indoor environments is referred to as sick building syndrome (SBS) and is mainly caused by volatile organic compounds (VOCs) [1, 2, 3, 4, 5, 6]. Patients with SBS suffer from a variety of nonspecific symptoms such as irritation of the eyes, nose, or throat. Additionally, certain neurotoxic or general health problems present as skin irritations, with nonspecific hypersensitivity reactions including infectious diseases and odor and taste sensations [1, 2, 3, 4, 5, 6]. These patients also suffer from general fatigue. Many efforts have been directed at exploring the etiology of SBS, such as attempts to identify patients by certain genetic or psychological features [1, 2, 3, 4, 5, 6]. However, efforts to unambiguously account for the occurrence of this syndrome and strategies to prevent its occurrence by avoiding exposure to specific chemicals remain unclear [1, 2, 3, 4, 5, 6].
On the other hand, various attempts have been made to improve human health by modifying indoor air environments. For example, efforts have been devoted to increasing air tightness and thermal insulation properties to avoid marked changes between rooms [7, 8, 9, 10]. Additionally, antifungal measures are also important since a variety of fungi can cause health problems such as hypersensitivity pneumonitis and other allergic diseases [11, 12].
In this chapter, two approaches to improve human health by indoor environment modifications are introduced. One approach involves “enhancement of natural killer cell activity caused by negatively charged particle dominant indoor air conditions,” while the other involves “improvement of pollen allergy symptoms by cloth containing specific ore powder.”
2. Enhancement of natural killer cell activity caused by negatively charged particle dominant indoor air conditions
We previously described the construction of negatively charged particle dominant indoor air conditions (NCPDIAC) [13]. Thereafter, the effects of NCPDIAC on human health have been monitored under short- (2.5 hours), middle- (2-week night stay), and long-term (3-month period of continuous residence) stays [13].
As shown in Figure 1A, the NCPDIAC apparatus consists of two components. One comprises the use of extra-porous charcoal paint [13]. This mainly induces dehumidification and deodorization. The important component that enhances natural killer (NK) cell activity comprises an electric voltage on the wall surface (72–100 V) [14, 15]. This electric voltage creates a negative charge on the wall surface [13]. Thus, positively charged particles (approx. 20 nm in diameter) are adsorbed onto the wall surface, and negatively charged particles remain at random in the rooms. As a result, this device creates NCPDIAC.
As shown in Figure 1B–D panels, three different types of experiments were performed sequentially. In the first, 2.5 hour short-stay experiments were performed. At that time, three control rooms and three NCPDIAC rooms were built in the wide sub-underground laboratory in the Comprehensive Housing R&D Institute, Sekisui House Ltd., at Kyoto Prefecture, Japan. The control and NCPDIAC rooms were 9.1 m2 (floor area) and 22.8 m3 (air volume). As described in Figure 1B, 60 volunteers occupied the control or NCPDIAC rooms for a 2.5 hour stay (short-term). There were no differences in temperature, humidity, or concentration of VOCs between control and NCPDIAC rooms during the experimental period. However, the concentration of charged particles differed [13]. As shown in Figure 1B, the concentration of positively charged particles in control rooms was slightly but significantly higher than that of negatively charged particles. It was considered that this difference may represent ordinary conditions. However, in NCPDIAC rooms, the concentration of positively charged particles decreased (by adsorption onto the wall surface), whereas that of negatively charged particles remained unchanged. Thus, the difference in concentration between positively and negatively charged particles was significantly greater (approximately 500–800 particles/cm3 room air) [13].
A second series of experiments was performed comprising 2-week night stays [14]. Fifteen volunteers (all Japanese males) occupied dormitory or Sekisui House rooms for 3 months. At the mid-month period, participants moved into control rooms (no NCPDIAC apparatus), and all participants were now subject to the same conditions at this point in time [14]. However, participants did not know which of the rooms (control or NCPDIAC) they had initially occupied. Participants stayed for 2 weeks during the evenings (night stay) while receiving employee training during the daytime and then moved into NCPDIAC rooms for the following 2 weeks. Thereafter, participants returned to the rooms they had initially occupied. As with the 2.5 hour stay experiments, there were no differences in temperature, humidity, or concentration of VOCs between control and NCPDIAC rooms during the experimental period [14]. However, the concentration of charged particles differed. As shown Figure 1C, the concentration of positively charged particles decreased in the NCPDIAC rooms, and there was a significant difference between positively and negatively charged particle concentrations [14].
A third series of experiments was performed comprising 3-month stays [15]. The NCPDIAC apparatus was installed in the bedrooms or living rooms of newly built or renovated homes or condominiums. Seven volunteers participated. Volunteers would switch the NCPDIAC apparatus ON or OFF themselves every 3 months [15]. A total of 16 OFF to ON trials (ON trials) and 13 ON to OFF trials (OFF trials) were performed [15]. When the switch was OFF, there were no differences in concentration between positively and negatively charged particles, whereas when the switch was ON, the concentration of positively charged particles decreased, and there was a significant difference between positively and negatively charged particle concentrations [15], as shown in Figure 1D.
3. Biological effects of NCPDIAC
Prior to and following each of the stay periods (2.5 hour, 2-week night, and 3-month ON/OFF trials of NCPDIAC), biological measurements were performed [13, 14, 15].
In the 2.5 hour stay experiments, various general medical checks were performed such as peripheral blood counts, liver and kidney functions, lipids, minerals as well as immunoglobulin, and stress biomarkers (including serum cortisol, salivary immunoglobulin (Ig) A, chromogranin, and amylase), as well as a questionnaire given for mood, various autonomic nerve conditions (heart rate, blood pressure, body sway, and Flicker test), and blood viscosity. Cytokinesrelated to balance between T helper (Th) 1 and Th2 such as interferon (IFN)-γ, tumor necrosis factor (TNF)-α, and interleukin (IL)-2 for Th1, and IL-4, IL-6, and IL-10 for Th2 were also measured.. All variables were recorded as [post-stay]–[pre-stay] values. These values were compared between stays in control and NCPDIAC rooms [13]. As shown in Figure 2A, the most significant difference was found in the level of IL-2 [13]. Although the changes were very small, there was a significant difference between stays in control and NCPDIAC rooms. Additionally, statistical significance was observed for changes in IL-4 (higher in NCPDIAC rooms) and fluctuations in heart rate (lower in NCPDIAC rooms). However, the most noticeable difference was in IL-2 [13].
Two-week night-stay experiments were then performed. For this series of experiments, additional items that were checked included NK activity, urine 17-hydroxycorticosteroid (OHCS) as a stress marker, and deoxyguanosine (8-OHdG) as an oxidative stress marker, since it was considered that these factors may change during the 2-week period, even though they remain unchanged in the short term [14]. The only difference observed for the various biomarkers examined prior to and following occupation of the NCPDIAC rooms was in NK cell activity. As shown in Figure 2B, relative NK cell activity tended to increase with sample collection (SC) 3 (after a 2-week night stay in NCPDIAC rooms) and SC1 as 1.0, while a significant increase was observed with SC3 and SC2 as 1.0. This was considerable at this point, as the short-term experiments revealed a significant increase in IL-2 [14]. However, IL-2 levels were considered to return to basal levels after participants had ceased to occupy NCPDIAC rooms. The slight but significant increase in IL-2 levels during the nighttime for the 2-week period may lead to activation of NK cells [14].
The third series of experiments involved participants living in their own homes [15]. Participants had the NCPDIAC apparatus in their bedrooms or living rooms. This apparatus was switched ON or OFF every 3 months by the volunteers themselves. Biological measurements were performed prior to the ON period (including the initial pre-time) and 3 months later (just prior to the OFF period) and then again just prior to the ON period (3 months later). As shown in Figure 2C, relative NK cell activity increased during the ON period and decreased during the OFF period [15]. The left panel of Figure 2C shows a 3-month ON period, with both NK cell and target cell ratios (10:1 and 20:1, respectively) shown [15]. In both cases, after a 3-month ON period, the relative NK cell activity increased [15]. On the other hand, as shown in the right panel of Figure 2C, during the OFF period, even with cell ratios of 10:1 and 20:1, the NK cell activity decreased [15].
NK cell activity is known to be correlated with the presence of cancer cells in humans and with viral infection of cells. Thus, indoor environments that yield enhancements in NK cell activity may somehow lead to the prevention of cancers in occupants and improvement of symptoms associated with viral-mediated illnesses such as influenza.
4. Other findings regarding NCPDIAC
In addition to the aforementioned results, in vitro studies were performed [16]. Peripheral blood mononuclear cells from healthy volunteers were cultured in a standard CO2 incubator or with forced influx using an adsorbed negatively charged air incubator. With the latter (experimental) incubator, the concentration of negatively charged particles was higher, at approx. 3000 particles/cm3 air in the incubator [16].
It was found that NK cell activity was enhanced in the experimental incubator. Moreover, CD25 expression in CD4 T cells and IFN-γ production in supernatants were also enhanced following application of the experimental incubator. These findings also support the notion that NCPDIAC may stimulate the immune status, but not quite pathologically [16]. Then, to demonstrate a representative phenotype, NK cell activity was found to be enhanced as shown in Figure 2C.
Furthermore, in the 3-month stay experiments, serum amyloid A (SAA) levels decreased significantly during the ON period [17]. Although the exact meaning of this finding is unclear, SAA is considered to be an acute reactive protein such as C-reactive protein (CRP) [18]. Additionally, the increase in high sensitivity CRP is considered to represent a predictive biomarker of atherosclerosis, and, if SAA levels also fluctuate similar to CRP, NCPDIAC may prevent the progression of atherosclerosis [17].
At present, our efforts are being directed at monitoring participants engaged in living under NCPDIAC for greater than 1 year.
5. Improvement in pollen allergy symptoms by cloth containing specific ore powder
Next, a trial aimed at preventing pollen allergies by indoor environment modifications was introduced [18].
We used specific natural ore powder (SNOP) in the form of a cloth containing this powder (CCSNOP). Details of the experiments have been reported previously. SNOP was obtained near Mount Aso, one of the biggest volcanoes in Japan (Kumamoto Prefecture), and is known to release far-infrared rays [18]. Chemical analyses revealed no specific characteristics of the natural ore found surrounding the Mount Aso area and mainly comprise SiO2, Al2O3, Fe2O3, Na2O, and other small chemical compounds. The Cosmic Garden Co. Ltd., a custom-home building company located in Okayama City, Japan, is the company from which our materials are sourced [18]. Their products and homes contain features of “2 × 4” construction methods for aseismic capacity, the avoidance of chemical substrates and smells by well-sealed and super-insulated areas, and enhanced durability. Additionally, this company has employed SNOP within wall materials. Since clients utilizing these products have provided anecdotal accounts of improvements in symptoms related to pollen allergies, we attempted to investigate these phenomena and provide empirical evidence for any health benefits [18].
As shown in Figure 3, 20 pollen allergy patients were recruited in April (the season for pollen allergies in Japan) of 2014. The average age of participants was 36.9 ± 11.2 years and comprised of 11 males and 9 females [18]. Over a 2-week period, participants occupied rooms covered by CCSNOP or by non-woven cloth (NWC), which did not contain the ore powder, for 1 hour. During this 1-hour period, windows were opened for 1–2 minutes every 15 minutes to expose the rooms to pollen [18]. Prior to and following occupation of the rooms, participants completed a questionnaire regarding symptoms and mood (a POMS (profiles of mood status) questionnaire was employed), and a variety of blood tests were performed including peripheral blood counts, liver and kidney functions, minerals, specific Ig E for various allergens, and cytokines. The measured items were represented as [post-admission] – [pre-admission] [18].
The results of the questionnaire of symptoms and mood are shown in Figure 4. In the upper panel, it can be seen that nasal obstruction, lacrimation, and difficulty of daily life improved in participants occupying the CCSNOP rooms compared with those occupying the NWC rooms. However, eye redness became worse in participants occupying the CCSNOP rooms. In the lower panel, moods for “tension and anxiety,” “depression,” and “fatigue” improved in participants occupying the CCSNOP rooms compared with those occupying the NWC rooms. Additionally, total mood disturbance also improved. All of these statistical analyses employed the chi-square test [19].
Total Ig E was found to increase slightly but significantly in participants occupying the CCSNOP rooms compared with those occupying the NWC rooms. Moreover, the percentage of eosinophils also increased in participants occupying the CCSNOP rooms. The reason for the changes in IgE and eosinophils remains unclear. Our experiment comprised just a 1-hour stay. Thus, although symptoms and moods may change rapidly, IgE and eosinophils changes may require more time [19].
In future experiments we intend to make available bedrooms that can be utilized by participants with pollen allergy during spring (season of pollen allergies) for at least 2 weeks in an effort to further investigate changes in symptoms, moods, and biological factors.
6. Conclusion
We have presented the outcome of two different strategies aimed at improving human health by modification of indoor environments. A consideration of several factors is required to maintain human health and minimize physical and mental disturbances while indoors, including the avoidance of chemical substances such as VOCs and other chemicals. Future investigations will involve participants occupying variously modified rooms (including NCPDIAC and SNCBOP) for longer periods of time. These studies should contribute toward the creation of healthy indoor environments for human habitation.
Acknowledgments
All experiments presented in this chapter were approved by the Ethic Committee of the Kawasaki Medical School, Kurashiki, Japan, and written informed consent was obtained from all participants.
Conflicts of interest
For the NCPDIAC experiments, the Department of Hygiene, Kawasaki Medical School, obtained research funding from Sekisui House Ltd., Osaka, Japan, and from Yamada SXL Home (now known as Yamada Home) Co. Ltd., Takasaki, Japan. Additionally, the extra-porous charcoal paints were provided by Artech Kohboyu, Co. Ltd., Omura, Nagasaki, Japan. For the CCSNOP experiments, the Cosmic Garden Co. Ltd. provided the CCSNOP apparatus.
References
- 1.
Stolwijk JA. Sick-building syndrome. Environmental Health Perspectives. 1991; 95 :99-100 - 2.
Lyles WB, Greve KW, Bauer RM, Ware MR, Schramke CJ, Crouch J, et al. Sick building syndrome. Southern Medical Journal. 1991; 84 (1):65-71, 76 - 3.
Laumbach RJ, Kipen HM. Bioaerosols and sick building syndrome: Particles, inflammation, and allergy. Current Opinion in Allergy and Clinical Immunology. 2005; 5 (2):135-139 - 4.
Burge PS. Sick building syndrome. Occupational and Environmental Medicine. 2004; 61 (2):185-190 - 5.
Israeli E, Pardo A. The sick building syndrome as a part of the autoimmune (auto-inflammatory) syndrome induced by adjuvants. Modern Rheumatology. 2011; 21 (3):235-239. DOI: 10.1007/s10165-010-0380-9 - 6.
Norbäck D. An update on sick building syndrome. Current Opinion in Allergy and Clinical Immunology. 2009; 9 (1):55-59. DOI: 10.1097/ACI.0b013e32831f8f08 - 7.
Carrer P, Wolkoff P. Assessment of indoor air quality problems in office-like environments: Role of occupational health services. International Journal of Environmental Research and Public Health. 2018; 15 (4):E741. DOI: 10.3390/ijerph15040741 - 8.
Le Cann P, Paulus H, Glorennec P, Le Bot B, Frain S, Gangneux JP. Home environmental interventions for the prevention or control of allergic and respiratory diseases: What really works. The Journal of Allergy and Clinical Immunology. In Practice. 2017; 5 (1):66-79. DOI: 10.1016/j.jaip.2016.07.011 - 9.
Charpin D, Baden R, Bex V, Bladt S, Charpin-Kadouch C, Keimeul C, et al. Environmental home inspection services in Western Europe. Environmental Health and Preventive Medicine. 2011; 16 (2):73-79. DOI: 10.1007/s12199-010-0171-0 - 10.
Wolkoff P. Indoor air humidity, air quality, and health—An overview. International Journal of Hygiene and Environmental Health. 2018; 221 (3):376-390. DOI: 10.1016/j.ijheh.2018.01.015 - 11.
Riario Sforza GG, Marinou A. Hypersensitivity pneumonitis: A complex lung disease. Clinical and Molecular Allergy. 2017; 15 :6. DOI: 10.1186/s12948-017-0062-7 - 12.
Spagnolo P, Rossi G, Cavazza A, Bonifazi M, Paladini I, Bonella F, et al. Hypersensitivity pneumonitis: A comprehensive review. Journal of Investigational Allergology & Clinical Immunology. 2015; 25 (4):237-250 - 13.
Takahashi K, Otsuki T, Mase A, Kawado T, Kotani M, Ami K, et al. Negatively-charged air conditions and responses of the human psycho-neuro-endocrino-immune network. Environment International. 2008; 34 (6):765-772. DOI: 10.1016/j.envint.2008.01.003 - 14.
Takahashi K, Otsuki T, Mase A, Kawado T, Kotani M, Nishimura Y, et al. Two weeks of permanence in negatively-charged air conditions causes alteration of natural killer cell function. International Journal of Immunopathology and Pharmacology. 2009; 22 (2):333-342 - 15.
Nishimura Y, Takahashi K, Mase A, Kotani M, Ami K, Maeda M, et al. Enhancement of NK cell cytotoxicity induced by long-term living in negatively charged-particle dominant indoor air-conditions. PLoS One. 2015; 10 (7):e0132373. DOI: 10.1371/journal.pone.0132373 - 16.
Nishimura Y, Takahashi K, Mase A, Kotani M, Ami K, Maeda M, et al. Exposure to negatively charged-particle dominant air-conditions on human lymphocytes in vitro activates immunological responses. Immunobiology. 2015; 220 (12):1359-1368. DOI: 10.1016/j.imbio.2015.07.006 - 17.
Lee S, Yamamoto S, Nishimura Y, Matsuzaki H, Yoshitome K, Hatayama T, et al. Decrease in serum amyloid A protein levels following 3-month stays in negatively charged particle-dominant indoor air conditions. Biomedical and Environmental Sciences. 2018; 31 (5):335-342. DOI: 10.3967/bes2018.044 - 18.
Pepys MB, Baltz ML. Acute phase proteins with special reference to C-reactive protein and related proteins (pentaxins) and serum amyloid A protein. Advances in Immunology. 1983; 34 :141-212 - 19.
Lee S, Okamoto H, Yamamoto S, Hatayama T, Matsuzaki H, Kumagai-Takei N, et al. Biological effects of cloth containing specific ore powder in patients with pollen allergy. Biomedical and Environmental Sciences. 2016; 29 (8):563-573