NeuroLogicEvidence levels

Metabolic and immune · AAPB chapter 24

Immune function

Immune function and inflammatory response

Eight randomised trials suggest a favourable effect on immunity, especially in immunocompromised people — but biofeedback was always combined with other approaches. One separate randomised trial reports higher CD4+ counts after alpha training.

Updated :

What the research shows

EEG neurofeedback — standard amplitude training

Alpha-amplitude EEG neurofeedback — CD4+ counts in HIV-positive adults

Ages
Adult (18+)
Techniques
Alpha training

AAPB3Probably efficacious NeuroLogic3Probably efficacious same vs AAPB

Level 3 maintained. The AAPB's neurofeedback rating rests on a single trial: Schummer 2013 randomised 40 HIV-positive, AIDS-negative volunteers to neurofeedback, cranial electrotherapy, both, or a waitlist control (n = 10 per arm), gave the neurofeedback arms 20-minute twice-weekly sessions to raise eyes-closed alpha amplitude over 16 weeks, and found significant CD4+ increases in the neurofeedback and combined groups only, with the trained groups meeting their alpha amplitude target by the end of training. That is a randomised four-arm design with a documented learning check, but a single small study in one setting: Level 3, not Level 4. 2022-2026 window: Lubianiker 2026 randomised 85 healthy adults to fMRI neurofeedback upregulating reward mesolimbic activity, non-mesolimbic control-region upregulation, or no neurofeedback before hepatitis B vaccination; post-vaccination antibody levels did not differ between groups. That is a different technique in healthy volunteers, rated on its own row, and does not bear on the alpha-amplitude rating.

Other neurofeedback methods

fMRI neurofeedback — modulation of the immune response (adult)

Ages
Adult (18+)
Techniques
fMRI neurofeedback

AAPB0Not rated NeuroLogic1Not empirically supported

Level 1. New row: AAPB does not rate fMRI neurofeedback for immune outcomes. Lubianiker 2026 is the only study — a preregistered, double-blind trial randomising 85 healthy adults to reward mesolimbic upregulation (n = 34), non-mesolimbic control-region upregulation (n = 34) or no neurofeedback (n = 17) before hepatitis B vaccination. Both neurofeedback groups increased activation in their target region, and ventral tegmental area upregulation correlated with the post-vaccination rise in hepatitis B antibody (r = 0.31, P = 0.018); but the prespecified group comparison of antibody change was null, and no adverse effects occurred. A solid mechanistic demonstration in healthy volunteers, with a null outcome and no replication, supports nothing above Level 1.

Biofeedback

EMG and thermal biofeedback, HRV, within combined interventions — immune and inflammatory markers (adult)

Ages
Adult (18+)
Techniques
EMG biofeedback, Thermal biofeedback, HRV — resonance-frequency breathing

AAPB3Probably efficacious NeuroLogic3Probably efficacious same vs AAPB

Level 3 maintained. AAPB base: eight randomised trials in which biofeedback was one component of a relaxation package. Peavey 1985 (n = 16, EMG and thermal training) increased phagocytic capacity versus control; McGrady 1992 (n = 31 healthy adults, four sessions) increased T-lymphocyte blastogenesis and lowered white cell count versus a no-treatment group, with cortisol unchanged; Gruber 1993 (n = 13 post-mastectomy) increased natural killer cell activity, mixed lymphocyte responsiveness and peripheral blood lymphocytes versus delayed treatment; Taylor 1995 (n = 10 HIV-positive men) increased T-cell count, maintained at 1 month; Coen 1996 and Kern-Buell 2000 (mild asthma, n = 20 and n = 16) reduced asthma severity and medication use, with higher CD4+ and CD8+ counts in the first and a lower neutrophil percentage in the second; Birk 2000 (n = 31 with HIV) showed no group gains in CD4+, CD8+ or natural killer counts. Lehrer 2010 (n = 11) found less HRV reduction after an endotoxin injection but unchanged cytokines, and Nolan 2012 was inconclusive. 2022-2026 window: Herhaus 2023 randomised 55 people with panic disorder to four weeks of slow-paced breathing with HRV biofeedback or sham HRV biofeedback and reduced TNF-alpha (η² = 0.077), with no effect in the sham arm. Not Level 4: no trial isolates the biofeedback contribution.

In short

Clinical reading

AAPB Level 3; NeuroLogic Level 3 for biofeedback and for alpha neurofeedback alike. All eight biofeedback studies combined it with other components without isolating its contribution; several failed to demonstrate training success (lower EMG, higher hand temperature). The neurofeedback rating rests on Schummer 2013 alone (n = 40, alpha training, higher CD4+ counts). fMRI neurofeedback is rated separately at Level 1 on a single randomised trial with a null result.

Protocols

EMG- and temperature-assisted relaxation, resonance-frequency HRV; 6-10 session protocols within multimodal programmes. Neurofeedback: eyes-closed alpha amplitude, 20 minutes twice weekly over 16 weeks.

Limits

Clinical improvement (medication use, infections) is rarely measured; intermediate immunological markers dominate. The one sham-controlled result (Herhaus 2023) concerns a single cytokine in one setting; the fMRI trial was run in healthy volunteers with a null outcome. No paediatric data.

Study base

Eight RCTs plus two specific studies (HRV and endotoxin, neurofeedback and CD4+). 2022-2026 base: 2 publications indexed in the archive (1 HRV biofeedback, 1 fMRI neurofeedback).

Brendan's perspective

The same level as the AAPB on both rows, and I am comfortable there. Eight randomised trials, biofeedback bundled every time with relaxation, imagery or autogenic training, and several with no evidence that the training took at all — hand temperature did not rise in Coen 1996 or Kern-Buell 2000. When the manipulation check fails, the trial tells you about the package, not about the method. Schummer 2013 is better than its reputation: four arms, randomised, a documented alpha learning check, higher CD4+ counts in the trained groups. It is also still alone thirteen years later, with nothing replicating it. Lubianiker 2026 is a beautifully built fMRI study with a null primary outcome in healthy volunteers, which is science rather than a clinic option. In practice I approach immune physiology only through the front door — HRV biofeedback for autonomic regulation, sleep and stress — and I would not offer neurofeedback as training aimed at immune function. Nobody has yet shown a change in infections, medication use, or anything the patient would notice.

Read next on the NeuroBLOG

Brendan Parsons, Ph.D., BCN — Founder of NeuroLogic, neurofeedback practitioner and trainer in Nice, AAPB board member

Explore this condition in the tool Compare every condition

References cited

  1. McGrady et al. (1992) The effects of biofeedback-assisted relaxation on cell-mediated immunity, cortisol, and white blood cell count in healthy adult subjects doi:10.1007/BF00844727
  2. Lehrer et al. (2010) Voluntarily produced increases in heart rate variability modulate autonomic effects of endotoxin induced systemic inflammation: An exploratory study doi:10.1007/s10484-010-9139-5
  3. Schummer et al. (2013) The effect of neurofeedback and cranial electrotherapy on immune function within a group of HIV+ subjects: A controlled study doi:10.1080/10874208.2013.813168
  4. Herhaus et al. (2023) Effect of a slow-paced breathing with heart rate variability biofeedback intervention on pro-inflammatory cytokines in individuals with panic disorder - A randomized controlled trial doi:10.1016/j.jad.2023.01.091
  5. Lubianiker et al. (2026) Upregulation of reward mesolimbic activity and immune response to vaccination: a randomized controlled trial doi:10.1038/s41591-025-04140-5